Third Party Nutraceutical & Ayurvedic Manufacturer India | Shakumbhri Groups

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ISO 22000:2018 Certified Quality Standards
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Premium Herbal & Nutraceutical Manufacturing
Private Label & Contract Manufacturing Solutions
Global Export & Regulatory Support
500+ Herbal, Ayurveda & Nutraceutical Formulations
State-of-the-Art Manufacturing Technology
WHO-GMP Certified Manufacturing Facility
ISO 22000:2018 Certified Quality Standards
Advanced Research & Development
Premium Herbal & Nutraceutical Manufacturing
Private Label & Contract Manufacturing Solutions
Global Export & Regulatory Support
500+ Herbal, Ayurveda & Nutraceutical Formulations
State-of-the-Art Manufacturing Technology
Label Compliance for Ayurvedic & Nutraceutical Products – AYUSH & FSSAI India | Shakumbhri
Label Compliance Β· AYUSH Β· FSSAI Β· Export Labels

One Non-Compliant Label
Can Ground Your
Entire Launch.

Non-compliant product labels are the leading cause of marketplace delisting, drug authority notices, customs rejection, and product recall for Indian herbal and nutraceutical brands. Our label compliance team reviews every element of your label artwork before you go to press β€” eliminating risk before it becomes a crisis.

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AYUSH Compliant
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FSSAI Compliant
🌍
Export Label Review
⚑
72hr Turnaround
🚫
Prohibited Claims Audit
72 hrs
Review Turnaround
AYUSH
Schedule T Compliant
FSSAI
2022 Amendment
2025
QR Code Ready
Zero
Delisting Risk

Why Label Compliance Matters

The Most Avoidable
Brand-Killing Mistake

In 2024, the FSSAI conducted over 12,000 product enforcement actions against food supplement brands for labelling non-compliance. Amazon India delisted over 3,000 Ayurvedic and nutraceutical product listings for prohibited claims violations. Drug authorities in multiple Indian states issued show-cause notices to Ayurvedic brands for illegal disease-cure claims. Every one of these was avoidable with a proper label compliance review before printing.

The regulatory landscape for Ayurvedic and nutraceutical labelling in India is complex and regularly updated. The Drugs & Cosmetics Act Schedule T provisions, FSSAI Packaging and Labelling Regulations, the Drugs & Magic Remedies Act, Consumer Protection Act, and FSSAI’s 2022 nutraceutical labelling amendment all impose overlapping requirements and restrictions β€” and a single violation of any one of them is sufficient grounds for enforcement action.

Our label compliance review provides a comprehensive written report identifying every non-compliant element, every prohibited claim, every missing mandatory declaration, and every formatting requirement violation β€” along with specific corrected wording and artwork guidance so your printer receives a submission-ready file.

What Our Label Review Covers

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AYUSH Mandatory Elements
Botanical name, plant part, license numbers, net content, classical reference
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FSSAI Nutraceutical
Nutrition info panel, ingredient order, allergen statement, FSSAI license
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Prohibited Claims
D&C Act, Magic Remedies Act, Amazon/Flipkart claim policies
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Export Label Adapt.
EU, USA, GCC, ASEAN market-specific labelling requirements
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QR Code 2025
Mandatory AYUSH batch-traceable QR implementation
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Packaging Compliance
EPR declarations, BIS symbols, plastic waste management

Quick Reference

Mandatory Label Elements:
AYUSH vs. FSSAI

Label ElementAYUSH (Ayurvedic)FSSAI (Nutraceutical)
Product Nameβœ” Mandatoryβœ” Mandatory
Ingredient Listβœ” Botanical name + plant partβœ” Descending order by weight
AYUSH License Numberβœ” MandatoryNot applicable
FSSAI License NumberNot applicableβœ” Mandatory
Nutritional Information PanelOptionalβœ” Mandatory
Allergen DeclarationRecommendedβœ” Mandatory where applicable
Classical Text Referenceβœ” Required (classical formulas)Not applicable
Disease Cure Claimsβœ— Prohibitedβœ— Prohibited
QR Code (2025 mandate)βœ” MandatoryStrongly recommended
Best Before / Expiryβœ” Mandatoryβœ” Mandatory

Get Your Label Reviewed

72-Hour Label
Compliance Review

Submit your label artwork. Within 72 hours, receive a written compliance report with every issue identified, specific corrected language provided, and regulatory citation for each point. The most valuable 72 hours before your print run.

COA Documentation β†’

Download Free Product Catalogue

Get instant access to 500+ Ayurvedic and Nutraceutical formulations with MOQ, pricing guidance, and regulatory checklist β€” delivered as a PDF to your inbox.

Your details are secure and will never be shared with third parties.
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Review Before You Print.
Not After You’re Listed.

72-hour label compliance review. The cost of a review is a fraction of a single marketplace delisting, product recall, or regulatory notice.

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