Manufacturing Capability · Tablets

Ointment, Cream & Gel Manufacturing in Delhi NCR

Dermatological, herbal, ayurvedic and pain-relief topicals — manufactured in our WHO-GMP certified facility with controlled emulsification, stability-tested formulations, and precise fill accuracy. Private label and contract manufacturing both available.

WHO-GMP

Certified

ISO 9001:2015

Certified

FSSAI

Approved

AYUSH

Approved

100%

Quality Assurance

10+

Product Categories

500+

Products

100+

Brands

10+

Years Experience

Ointment, Cream & Gel Manufacturing

Topical formulations look simple in the finished tube — smooth, uniform, easy to apply. What most people don’t see is how unforgiving the manufacturing process actually is. An emulsion that separates on the shelf, a gel that turns cloudy after three months, or a cream that changes viscosity between batches — these aren’t cosmetic issues, they’re formulation and process failures that show up well after the product has already shipped. Getting topicals right requires controlling emulsification temperature, mixing sequence, and stability from day one of production, not catching problems after the fact.
Our ointment, cream and gel manufacturing facility in Delhi NCR handles dermatological formulations, herbal and ayurvedic topicals, pain relief gels, and cosmeceutical creams — all manufactured under WHO-GMP compliance with vacuum homogenization for stable emulsions and in-house stability testing before any batch clears for dispatch. If you’ve been searching for ointment manufacturing in India or a third party gel manufacturing partner that treats topicals with the same rigour as tablets and capsules, this is what that actually looks like on the production floor.
Whether you’re launching a private label pain relief gel, a herbal ayurvedic ointment, a dermatological cream formulation, or a cosmeceutical topical under your own brand — the manufacturing discipline and QC standard apply equally across all three categories.

Ointment vs Cream vs Gel — What's the Actual Difference

These three terms get used loosely in casual conversation, but they represent genuinely different formulation bases with different manufacturing requirements. Choosing the right base for your product isn’t just a texture preference — it affects how the active ingredient is delivered, how the product feels on skin, and what conditions it’s best suited for.

Ointments

Oil-based, typically petrolatum or similar hydrocarbon base with little to no water content. Greasy texture, occlusive — forms a barrier on skin that locks in moisture. Best for dry, cracked, or very irritated skin conditions where barrier protection matters.

Creams

Oil-in-water or water-in-oil emulsions — a genuine mix of oil and water phases stabilised with emulsifiers. Lighter than ointments, absorbs more readily, less greasy. The most versatile base — used across dermatological, cosmeceutical, and general skincare applications.

Gels

Water-based (or alcohol-based) with a gelling agent providing structure — no oil phase in most formulations. Fast-absorbing, non-greasy, cooling sensation on application. Common for pain relief products, acne treatments, and formulations needing quick skin penetration.

Choosing between these three isn’t arbitrary — it depends on your active ingredient’s stability and solubility, the skin condition you’re targeting, and how your brand wants the product to feel. If you’re unsure which base fits your formulation concept, tell us the active ingredient and intended use, and we can recommend based on manufacturing feasibility and typical market positioning for that category.

The Manufacturing Process — Formulation to Fill

Raw Material Testing & Phase Preparation

Actives and excipients are tested for identity and purity. Oil phase and water phase (for creams) are prepared separately and heated to matched temperatures — this temperature matching is critical for a stable emulsion, and mismatched phases are one of the most common causes of separation later.

Emulsification / Gel Formation

For creams, the water phase is added to the oil phase (or vice versa, depending on formulation type) under controlled vacuum homogenization — this creates a stable emulsion without incorporating air, which causes texture and stability problems. For gels, the gelling agent is hydrated and dispersed under controlled shear to achieve uniform viscosity.

Active Ingredient Incorporation

Active pharmaceutical or herbal ingredients are added at the correct process stage and temperature — some actives degrade at high temperatures and must be added during the cooling phase, not the initial mixing. Getting this sequence wrong reduces potency even if every other step is correct.

Cooling Under Controlled Vacuum

The batch is cooled gradually under continued vacuum mixing to prevent air incorporation and to allow the emulsion or gel structure to stabilise properly. Rushing this stage is a common cause of texture inconsistency between batches.

In-Process & Stability QC

pH, viscosity, homogeneity, and appearance are tested before the batch is released for filling. Accelerated stability samples are pulled from the batch and placed under controlled storage conditions to monitor for separation, colour change, or potency loss over time.

Filling in Your Branded Packaging

QC-cleared product is filled into your branded tubes, jars, or bottles at controlled fill weight. Certificate of Analysis issued per batch. Dispatched PAN India with full batch documentation.

Have a Ointment Formulation to Manufacture?

Tell us your active ingredient, target base (ointment, cream or gel), and MOQ — we’ll confirm feasibility, pricing, and lead time within 24 hours.

Why Choose us for Ointment Manufacturing & Cream Manufacturing

Vacuum homogenization for genuinely stable emulsions

Air incorporation during mixing is a leading cause of cream separation and texture inconsistency. Our vacuum-controlled mixing process prevents this at the source, not through post-production fixes.

In-house accelerated stability testing

We don't wait for a customer complaint to find out a formulation separates after three months. Accelerated stability samples are pulled and monitored from every new formulation before it goes into full production runs.

Pharma, herbal and ayurvedic topicals — same process discipline

An ayurvedic herbal ointment goes through the same temperature-controlled emulsification and QC testing as a pharmaceutical cream. We don't treat herbal formulations as a lower-rigour category.

Active ingredient sequencing handled correctly

Heat-sensitive actives are incorporated at the right process stage — not dumped in during initial high-temperature mixing where potency loss occurs. This is a detail that separates functioning topicals from ones that fail assay testing.

Multiple packaging formats from one facility

Tubes, jars, and airless pump bottles — all available without needing a separate packaging contractor. Your finished, branded, QC-cleared product dispatches from a single location.

WHO-GMP ointment manufacturer — consistent standard regardless of batch size

As a cream manufacturing company Delhi NCR brands trust, and a private label cream manufacturer for brands across categories, small first-order clients and established recurring brands get the same manufacturing process and QC discipline. Certificate of Analysis issued automatically with every batch.

Quality Control and Stability Testing

Topicals fail differently than tablets or capsules — separation, colour change, and consistency drift are the main failure modes, and they don’t always show up on day one. Our QC and stability process is built specifically around catching these before they reach the market.
Test Parameter What It Confirms
pH Testing Product is within the correct range for skin compatibility and active ingredient stability
Viscosity Consistent texture batch-to-batch — matches the approved reference standard
Homogeneity No visible particles, streaking, or phase separation in the finished product
Assay (Active Ingredient Potency) Active ingredient content matches label claim within accepted limits
Accelerated Stability Testing Product monitored under controlled temperature/humidity conditions to predict shelf-life performance
Microbial Limits Bioburden within acceptable limits — critical for water-containing formulations prone to microbial growth

Ointment, Cream & Gel Manufacturing — FAQ

MOQ typically starts from 3,000 to 5,000 units per SKU depending on tube or jar size. Batch size minimums also apply — generally starting from around 20 to 25 kg per formulation for a first production run. If you’re testing a new product concept with a smaller initial order, share your target quantity and we’ll confirm what’s realistically workable.
It depends on your active ingredient’s solubility and stability, the skin condition being targeted, and how you want the product to feel on application. Oil-soluble actives with a barrier-protection goal often suit ointments. Most general dermatological and cosmeceutical products work well as creams. Fast-absorbing, non-greasy applications — pain relief, acne treatment — typically work better as gels. Tell us your active ingredient and intended use and we’ll recommend based on manufacturing feasibility.
Yes — for new formulations, we pull accelerated stability samples and monitor them under controlled temperature and humidity conditions before committing to a full production run. This catches separation, colour change, or potency drift issues at the formulation stage rather than after a large batch has already been manufactured and shipped.
Yes — herbal and ayurvedic ointments, creams, and gels are manufactured under AYUSH-compliant protocols with botanical authentication of the raw herbal extracts, alongside the standard physical, chemical, and microbial QC panel applied to all our topical formulations. The rigour is the same as our pharmaceutical topical products.
For an existing formulation with approved packaging artwork, typically 15 to 25 working days from documentation and artwork sign-off to dispatch. New formulations requiring stability testing before full production add time for that testing cycle. Repeat orders on locked formulations and artwork move faster, generally 10 to 15 working days.

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