Fruit & Vegetable Fertiliser | Organic Plant Food 4-5-6
A balanced 4-5-6 feed for fruit and veg.
from £11.50

Dr Forest Rose & Shrub Fertiliser is a slow-release organic coarse powder handcrafted in Stockport, Greater Manchester, for roses and flowering shrubs — hydrangeas, camellias, rhododendrons, azaleas and the deciduous shrubs that carry the summer garden. The 5-3-5 NPK ratio balances vigorous cane and stem growth with the sustained potassium supply needed for bloom production, colour intensity, fragrance and repeat performance across a full season — without the high-nitrogen excess that pushes leafy growth at the expense of flowers.
From first bud break in March to the final autumn flush — premium organic ingredients working across the full season. Fermented biochar and EM microorganisms improve soil biology permanently with every application. Yorkshire Polyhalite delivers four nutrients simultaneously from a single North Yorkshire mineral. Alfalfa Meal contributes triacontanol, the natural compound prized by rose growers for its effect on bud count and fragrance intensity. The blend is pH-neutral, so it feeds acid-loving shrubs such as camellias and rhododendrons without liming the soil they sit in. This is a fertiliser that improves the soil it feeds, not just the plants above it.
Unlike fruiting plants that benefit from a high K:N ratio (2:1 or more), roses and flowering shrubs simultaneously produce substantial vegetative structure — canes, stems, laterals, leaves — and flowers across a long season. Equal N and K at 5% provides the balanced support for both. Phosphorus is intentionally modest at 3%: established woody plants have deep root systems and do not need high P, and excess phosphorus in the slightly acidic soils roses and most flowering shrubs prefer can interfere with micronutrient uptake. It is also the reason a low-P blend is the sensible choice around hydrangeas. This is a formula calibrated for how these plants actually grow — not derived from a general-purpose template.
The 5-3-5 ratio suits general flowering-shrub feeding, and it suits pink and white hydrangeas well. Blue is a different question, and it is worth being plain about it. Blue hydrangea colour depends on acidic soil and on aluminium being present in a plant-available form — it is not something an NPK ratio delivers. Phosphorus is the classic antagonist: it binds aluminium in the soil and takes it out of circulation, which is the usual reason blueing fails on a high-phosphorus feed. At 3% P this blend is modest and will not work against you. But if blue flowers are the goal, the limiting factor is your soil pH, not your fertiliser. Bring pH down with our Sulphur Soil Acidifier, and see the full hydrangea and ericaceous range. This product feeds the plant; it does not change flower colour, and we do not claim that it does.
Every ingredient contributes a specific, research-backed function. The formula combines traditional organic inputs — long proven by rose growers — with premium regenerative ingredients that permanently improve soil biology. No fillers. Nothing inert.
Rates are calibrated for the 5-3-5 NPK formula and apply to roses and to flowering shrubs alike. All g/m² rates assume even surface distribution over the full root zone with light incorporation to 2–3cm depth. For new plantings or beds being prepared for the first time, apply at double the standard rate and work into the full planting depth before setting the plants in.
| Rose or Shrub Type | Rate per m² / plant | Applications per Season | Timing |
|---|---|---|---|
| Hybrid Tea roses | 80–100g per m² | 3–4 applications | Late March · late May · late June · early August (stop after early August) |
| Floribunda roses | 80–100g per m² | 3–4 applications | Late March · late May · late June · early August (stop after early August) |
| Shrub roses (incl. English roses) | 80–100g per m² | 3 applications | Late March · June · late July (stop after late July for most shrubs) |
| Climbing roses | 90–110g per m² | 3–4 applications | Late March · late May · late June · early September (wall warmth extends hardening) |
| Rambling roses | 80–90g per m² | 2 applications | Late March · immediately after flowering (July–August). Once-blooming — no mid-season feed needed. |
| Miniature roses | 50–65g per m² | 3–4 applications | Late March · May · July · early August. Lower rate due to smaller root zone. |
| Ground cover roses | 70–80g per m² | 2–3 applications | Late March · June · (optional) early August for repeat-flowering varieties |
| Hydrangea — mophead & lacecap (H. macrophylla) | 80–100g per m² | 2–3 applications | Late March · June. Stop after June — these flower on last year's wood and need the summer to ripen it. |
| Hydrangea — paniculata & arborescens | 80–100g per m² | 2–3 applications | Late March · late May · (optional) late June. These flower on current-season wood, so early feeding does the work. |
| Camellia | 80–100g per m² | 2–3 applications | Late March · after flowering (May–June). The post-flowering feed supports next year's bud set. |
| Rhododendron & azalea | 80–100g per m² | 2–3 applications | Late March · immediately after flowering (May–June). Scatter on the surface — do not fork in over shallow roots. |
| Deciduous flowering shrubs (philadelphus, weigela, buddleja, spiraea) | 80–100g per m² | 2–3 applications | Late March · June · late July for late-flowering shrubs. Spring-flowering shrubs: feed again straight after flowering. |
| Lilac, viburnum & other woody shrubs | 80–100g per m² | 2–3 applications | Late March · June. Established specimens are generally content with the March feed alone. |
| Situation | Initial Charge | Top-Dress | Notes |
|---|---|---|---|
| Pots & containers | 3–4g per litre of compost | 2g per litre · every 4 weeks | Mix the initial charge evenly through the full compost volume before planting. 3g/L for compost already containing slow-release nutrients; 4g/L for plain or peat-free mixes. |
| Standard rose or shrub pot (15–20L) | 45–80g | 30–40g · every 4 weeks | Apply around the inner perimeter of the pot, not mounded at the stem base. The same applies to potted hydrangeas, camellias and patio shrubs. |
| Situation | Rate | Method |
|---|---|---|
| Bed preparation (pre-planting) | 100–140g per m² | Fork into the top 15–20cm before planting. This charges the root zone before the plant goes in — particularly important in rose beds and shrub borders that have not been fed for several seasons. |
| Individual planting hole | 30–50g per plant | Mix into the soil removed from the planting hole before backfilling. Do not place fertiliser in direct contact with the roots — mix thoroughly with soil first. |
Roses have a reputation for being difficult, and flowering shrubs a reputation for looking after themselves. Neither is quite right. In practice the basics are straightforward — and understanding them makes the difference between a plant that survives and one that thrives. This guide covers the main rose types, the flowering shrubs most often grown alongside them, the seasonal feeding rhythm, and what to watch for through the year.
Roses fall into a small number of groups with meaningfully different growing habits. Knowing your type helps you feed and prune at the right time. Flowering shrubs are covered in the section below this one.
Flowering shrubs divide most usefully by where the flowers come from. A shrub that flowers on wood made last year needs its feeding finished early enough for that wood to ripen; a shrub that flowers on this year's growth can be fed later. Get that one distinction right and the rest follows.
Mophead and lacecap hydrangeas turn blue when the soil is acidic — roughly pH 5.5 and below — and aluminium is present in a form the roots can take up. Above that, the same plant flowers pink. White varieties stay white whatever you do. Phosphorus is the antagonist in this: it binds aluminium into insoluble compounds and takes it out of reach, which is why a high-phosphorus feed is the usual reason blueing fails. At 3% P this blend is modest and will not obstruct you, but it is a fertiliser, not a colourant, and it will not turn a pink hydrangea blue on its own. If blue is the goal, the work is in the soil: lower the pH with our Sulphur Soil Acidifier and keep it there, and see the hydrangea and ericaceous range for the rest.
Timing matters as much as rate. The calendar below is built around roses, which have the longest feeding season of anything in this group; the notes say where flowering shrubs and hydrangeas step off it.
| Month | What the Plant is Doing | Feeding Action | Notes |
|---|---|---|---|
| January–February | Dormant. No leaf, minimal root activity. | Do not feed. | Use this time to prune (late February for most), clear old mulch, and check for overwintering pests and disease debris. Apply a fresh mulch of well-rotted compost after pruning. Leave last year's hydrangea heads on until the worst frosts have passed — they shelter the buds beneath them. |
| Late March | First red buds breaking. Root activity resuming. | First feed of the season. | The trigger is bud break — visible red buds emerging from the canes. Apply around the drip line at the full season rate. This is the most important application of the year — it charges the root zone before the main growth flush begins. Flowering shrubs, hydrangeas included, take their first feed at the same point. |
| April–May | Rapid cane and leaf extension. Bud initiation. | No feed needed if late March was done. | Watch for aphids on soft new growth — the chitin in Mealworm Frass will be priming SAR responses but this takes a few weeks. A seaweed liquid spray (not this product) can boost the SAR activation. Check soil moisture and water deeply if dry. |
| Late May | Buds swelling. First flush approaching. | Second feed (4–5 weeks after March). | Critical timing — nutrients applied now will be available in the flower itself. This application directly determines bloom size, petal substance and fragrance intensity in the first flush. Do not skip this one. Hydrangea paniculata and arborescens take their second feed here, since they flower on the growth they are making now. |
| June | Main flush flowering. Deadheading begins. | No feed during peak flowering. | Deadhead spent flowers promptly — removing the developing hip redirects the plant's energy from seed production back to bud initiation. On ramblers, note which canes are carrying flowers this year: these will be removed after flowering, not next spring. |
| Late June | First flush ending. New basal shoots emerging. | Third feed (4–5 weeks after May). | This feed sustains the new basal shoots — the strong new canes from the base of the plant — which will carry next year's best flowers. It also initiates the second flush of bloom in repeat-flowering varieties. Ramblers: feed immediately after flowering instead. Mophead and lacecap hydrangeas: this is their last feed of the year, so the wood ripens before autumn. |
| July | Second flush developing. New canes extending. | No feed unless 5 weeks since last application. | A hot, dry July can cause stress — water deeply at the base rather than splashing foliage. Fungal diseases spread rapidly in humid conditions; ensure good airflow around the plant and remove any heavily infected leaves at the compost bin, not the compost heap. |
| Early August | Peak repeat-flowering. Late basal shoots. | Fourth feed (optional — for repeat-flowering roses only). | This is the last feed of the season for most garden roses. It sustains the late summer and early autumn flowering. Once-blooming roses (ramblers, some old garden roses) do not need this application, and neither do flowering shrubs — they should already have finished. |
| Mid-August onwards | Late season flushes. Canes beginning to harden. | Stop all feeding. | Late feeding is one of the most common mistakes with roses, and with shrubs it is worse — a hydrangea that goes into autumn with soft, unripened wood loses next year's flower buds to the first hard frost. Late feeding produces growth that cannot harden before the first frosts, and that frost-killed growth provides entry points for disease and dieback. Let the plant transition naturally into autumn dormancy from mid-August. |
| September–November | Last flushes. Hips developing. Leaves yellowing. | Do not feed. | Some roses produce attractive hips in autumn — if you want these, stop deadheading in September and let the last flowers set fruit. Clear fallen leaves promptly as they can harbour black spot spores. Do not compost infected leaves. |
| December | Dormant. | Do not feed. | A good time to order bare-root roses and bare-root shrubs for planting in January–March. Bare-root stock is the best-value way to build a rose garden or a shrub border — it establishes faster than containerised plants and is significantly cheaper. |
The 5-3-5 ratio is not a generic template. It reflects the nutritional reality of how roses and flowering shrubs grow — producing both a substantial woody structure and flowers simultaneously across a season that runs from March to October in the UK.
Floral fragrance in roses is produced by volatile terpenoid and benzenoid compounds synthesised in the petal tissue. The terpenoid pathway — which produces the monoterpene geraniol, the sesquiterpene germacrene D, and related rose scent compounds — is potassium-dependent: K activates the enzymes and ATP-producing proton pumps required for terpenoid biosynthesis. Plants with inadequate K or with K supplied from chloride sources produce measurably lower concentrations of these compounds.
Every gram of K in this formula comes from chloride-free sources — Sulphate of Potash and Yorkshire Polyhalite. Muriate of potash (potassium chloride), the dominant K source in most garden fertilisers, delivers Cl⁻ ions that compete with K⁺ at cellular transporters and suppress secondary metabolite synthesis. The fragrance gap between roses fed with chloride-free K formulas and those fed with standard fertilisers is not subtle to anyone who grows both.
Triacontanol is a naturally occurring fatty alcohol present in Alfalfa Meal, first identified as a plant growth regulator in the 1970s by Ries and Houtz. Its mechanism involves activation of adenylate cyclase, raising intracellular cAMP levels and triggering cascades that increase the rate of meristematic cell division and secondary metabolite synthesis simultaneously. In rose-specific research, triacontanol application consistently increases the number of axillary buds that break and develop into flowering laterals — translating directly into more flowers per plant per flush. Professional rose growers have used alfalfa meal as a component of feeding programmes for decades; this formula incorporates it as a core ingredient.
Calcium is a structural component of pectin in cell walls. In rose petals, adequate Ca means walls with sufficient rigidity to maintain petal form throughout the life of the flower — in the garden and after cutting. Low Ca produces petals that lose form rapidly, bruise easily, and absciss prematurely. Gypsum provides immediately available Ca; Yorkshire Polyhalite provides sustained Ca across 50–60 days. The combination ensures Ca is continuously available across the full flowering season, not just immediately after application.
At 5% N, this formula is at the moderate end of the range for established roses. This is deliberate. Excess nitrogen in roses produces the conditions that create serious problems: the sappy, soft new growth that aphids colonise; the dense, poorly aerated canopy that creates the humid microclimate in which black spot and powdery mildew spread most rapidly; and the vigorous vegetative growth that produces canes and leaves at the expense of bud initiation. The organic nitrogen fractions in this formula mineralise progressively over 6–8 weeks — there is no nitrogen spike, no flush of sappy growth, and no sudden drop. The plant receives a consistent, moderate N supply that sustains growth without overwhelming it.
Chitin — present in Mealworm Frass — is detected by pattern recognition receptors in plant cell membranes as a marker of fungal presence or insect feeding. Detection triggers a signalling cascade that activates Systemic Acquired Resistance pathways throughout the plant: salicylic acid accumulates, defence genes are upregulated, and the plant's capacity to mount rapid responses to subsequent pathogen attack is enhanced for weeks. For roses, which face consistent pressure from three major fungal pathogens, this priming effect is meaningfully useful — it does not prevent infection, but it significantly reduces the severity and spread of the diseases that inevitably arrive in a UK summer.
Sepal colour in Hydrangea macrophylla is produced by a single anthocyanin, delphinidin-3-glucoside. On its own that pigment is pink. It turns blue only when it forms a complex with an aluminium ion, stabilised by co-pigments in the sepal tissue. So the question is never what pigment the plant makes — it always makes the same one — but whether aluminium reaches the sepal in a form that can complex with it.
That comes down to two things, and neither of them is the NPK ratio on the bag. The first is soil pH: aluminium is soluble and root-available below roughly pH 5.5, and progressively locked up as pH rises. The second is phosphorus. Phosphate reacts with aluminium in the soil to form insoluble aluminium phosphate, removing it from solution — which is why a high-phosphorus feed is the most common reason a blueing programme quietly fails. At 3% P this formula sits at the modest end and will not work against an acidification programme, but we are not going to claim more than that: this is a fertiliser, and it does not change flower colour. If blue is the goal, the intervention is soil pH, applied with a sulphur-based acidifier and maintained over time. Pink and white hydrangeas, and the paniculata and arborescens types, are unaffected by any of this and simply want feeding.
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