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Frequently Asked Questions

Find immediate, expert answers to common inquiries. Can't find what you need? Use our instant request portals at the bottom of the page.

What is the shelf life of your products?

Shelf life depends on the category and formulation:

The exact expiry depends on the composition and packing, and is confirmed by stability study before it is printed on the pack.

Do you have an in-house R&D facility?

Yes, we have a dedicated R&D and product-development capability that supports new product formulation and concept development, improvement of an existing formulation, product customisation and ingredient selection, flavour development, dosage-form development, trial and sample development, and packaging compatibility evaluation.

The aim is to turn your product concept into something that can actually be manufactured commercially — at the right cost, with the right stability.

Do you have FSSAI approval and a drug licence?

Yes. We hold FSSAI approval for our nutraceutical and food supplement range, and a valid drug licence for our pharmaceutical range.

Our manufacturing facility at Derabassi, Punjab is WHO-GMP certified and operated to US FDA compliant standards, with Halal and Kosher certification also in place. Copies can be seen on our certifications page.

Is your factory US FDA approved?

Our facility is built and operated to US FDA compliant standards and is WHO-GMP certified.

Compliance means the plant follows those manufacturing standards; it is not the same as a US FDA product approval, which applies to individual drug products. All certificates can be viewed on our certifications page.

Do you provide a Certificate of Analysis with each batch?

Yes. A Certificate of Analysis is issued for every batch, showing the batch number, manufacturing date, expiry date and test results. Batch manufacturing records are maintained for every production run.

Can I supply my own packaging material?

Yes, you can supply your own packaging material and we will manufacture with it.

Before printing, we provide the CDR artwork file so that the mandatory details — licence number, manufacturer name and address, and other regulatory content — can be verified and placed correctly. This step protects you, because incorrect statutory details on a pack cannot be fixed after printing.

Do you deliver across India?

Yes, we supply across India from our WHO-GMP certified unit at Derabassi, Punjab. The expected dispatch and delivery timeline is confirmed with you at the time of order confirmation.

Can you manufacture syrups, drops and oral liquids?

Yes — syrups, dry syrups, drops, oral suspensions, juices and shots, filled in PET and glass liquid bottles with measuring cups or droppers.

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