Delhi · Gurugram · Bangalore · Baddi · Bahadurgarh

Nutraceutical Label Claims Verification | FSSAI 2016 | NABL Accredited

An unverified or under-strength claim on a health supplement label exposes the brand to FSSAI surveillance action under Section 53 of the FSS Act, marketplace delisting across Amazon, Flipkart, Blinkit, Zepto, and BigBasket, and CCPA misleading-advertisement notices. Backed by the Arbro Group's unbroken NABL accreditation since 2003, Auriga Research delivers analytical label claims verification for every nutrient and active declared on your supplement label.

Label claim substantiation is governed by the FSS (Health Supplements, Nutraceuticals, Food for Special Dietary Use, FSMP, Functional Food and Novel Food) Regulations 2016 together with the FSS (Labelling and Display) Regulations 2020. Our scope spans water-soluble and fat-soluble vitamins by HPLC, B12 and folate by microbiological assay, minerals by ICP-OES / ICP-MS, omega fatty acid profiles by GC-FID, amino acids by amino acid analyser, botanical actives (curcuminoids, withanolides, ginsenosides) by HPLC and LC-MS, and probiotic viable counts by selective media.

For nutrients claimed on the label, FSSAI requires an analytical floor of 80% of declared through shelf life — our reports include per-serving and per-dose figures formatted for direct paste into your CoA and label dossier.

Reports in 10–14 working days | Express: 7 days available
Get a Quote Call +91-7428116100

Testing Parameters

Each parameter is mapped to its validated method so QA and labelling teams can match scope to declared label claims at a glance.

HPLC

Water-Soluble Vitamins

Vitamin C (ascorbic acid) and B-complex (B1, B2, B3, B5, B6, B9 folate, B7 biotin) by HPLC-UV / HPLC-DAD against pharmacopoeial standards.

HPLC

Fat-Soluble Vitamins

Vitamin A (retinol, beta-carotene), D2/D3, E (tocopherols), K1/K2 by HPLC-UV / HPLC-FLD with saponification step for ester-form claims.

Microbiological

Vitamin B12 & Folate

Microbiological assay using Lactobacillus delbrueckii (B12) and Lactobacillus rhamnosus (folate) — required where HPLC sensitivity is below FSSAI claim thresholds.

ICP-OES / ICP-MS

Mineral Quantification

Calcium, iron, zinc, magnesium, potassium, copper, manganese, selenium, chromium, and molybdenum by ICP-OES (mg-level) or ICP-MS (trace μg-level).

GC-FID

Omega Fatty Acid Profile

EPA, DHA, ALA, GLA, total omega-3 / 6 / 9 by GC-FID per AOAC 991.39. Required for fish oil, krill oil, flax oil, and chia-seed-derived supplements.

Amino Acid Analyser

Amino Acid Profile

20 protein-bound and free amino acids by HPLC post-column ninhydrin or amino acid analyser — for BCAA, whey, plant-protein, and sports nutrition products.

LC-MS

Botanical Actives

Curcuminoids (curcumin, demethoxycurcumin), withanolides (ashwagandha), ginsenosides (Rg1, Rb1, Re), bacosides (brahmi), gymnemic acid by HPLC-UV / LC-MS.

Plate Count

Probiotic Viable Counts

Strain-specific colony counts (Lactobacillus, Bifidobacterium, Bacillus, Saccharomyces) by selective media — supports CFU declaration on probiotic labels.

HPLC

CoQ10 & Lipoic Acid

Coenzyme Q10 (ubiquinone, ubiquinol) and alpha-lipoic acid by HPLC-UV — for cardiovascular and antioxidant supplement claim verification.

HPLC

Carotenoids & Lutein

Lutein, zeaxanthin, lycopene, astaxanthin, beta-carotene by HPLC-UV / HPLC-DAD for eye-health and antioxidant supplement claims.

Spectrophotometry

Protein Content

Total protein by Kjeldahl (AOAC 928.08) or Lowry / BCA where Kjeldahl is unsuitable — supports whey and plant-protein label claims.

HPLC

Choline, Inositol, Taurine

Choline, inositol, taurine, and L-carnitine by HPLC-ELSD / HPLC-UV — required where specialised actives are part of the label declaration.

How It Works

1

Get a Quote

Share your product type and the parameters you need tested. Your dedicated SPOC will confirm the testing scope, the applicable method, and the exact sample quantity required for your specific panel before you dispatch anything.

2

Send Your Sample

Dispatch your sample with a completed Test Request Form to the nearest Auriga lab. Each sample is individually bar coded and registered in YLIMS, Auriga's in-house Laboratory Information Management System, upon receipt. Testing begins within 24 hours of sample registration.

3

Testing and QA Review

Your sample is tested against the confirmed validated method by Auriga's scientific team. Every result passes through a formal internal QA review and sign-off before the report is generated.

4

Receive Your NABL Report

Your NABL-accredited test report is delivered digitally within the committed turnaround time. Reports carry Auriga's NABL accreditation under ISO/IEC 17025:2017 and are accepted by FSSAI under the Health Supplements Regulations 2016, BIS, and international buyers. You can track your sample status in real time through YLIMS at any point in the process.

Turnaround Time

Panel Standard TAT Express
Single-claim panel (1 vitamin or 1 mineral) 5–7 working days 3 days
Multi-vitamin / multi-mineral panel (10–18 claims) 10–14 working days 7 days
Omega fatty acid profile (EPA / DHA / ALA) 7–10 working days Available
Amino acid profile (20 AAs) 10–14 working days On request
Botanical actives (curcumin, withanolides, ginsenosides) 10–14 working days Available
Full combined claim panel (vitamins + minerals + amino acids + probiotics) 14–18 working days On request

Who Needs This Testing

  • D2C health supplement and nutraceutical brands launching on Amazon, Flipkart, Blinkit, Zepto, and BigBasket — all marketplaces now require analyst-verified claim data before listing.
  • Nutraceutical manufacturers preparing FSSAI Form B nutraceutical licence applications and renewals under the Health Supplements Regulations 2016.
  • Sports nutrition and weight-management brands needing BCAA, whey protein, and amino acid claim substantiation for label declarations.
  • Omega-3, fish oil, and krill oil brands requiring EPA / DHA quantification by GC-FID against label claims (typically 60% omega-3 of total fatty acids).
  • Ayurvedic and botanical-based supplement brands needing standardised actives (curcumin, withanolides, bacosides) at declared concentration through shelf life.
  • Brand owners contesting a marketplace delisting, FSSAI surveillance finding, or distributor dispute with an NABL-accredited counter-report.
  • Reformulators verifying that a recipe or supplier change still meets the label claim through stability (works alongside our stability testing service).

Why Auriga for Label Claims Verification

Unbroken NABL accreditation since 2003

Arbro Group has held NABL ISO/IEC 17025 accreditation continuously since 2003 — the audit trail FSSAI, marketplaces, and procurement teams look for.

Dual NABL + FSSAI notification

Reports carry evidentiary weight under the FSS Act 2006 Section 53 (Misleading Advertisement) for nutraceutical licence applications and marketplace listing reviews.

Label-ready output, not raw data

CoAs include per-serving and per-dose values formatted for direct paste into your label and Form B dossier — no separate formatting step on your side.

Full panel under one roof

Vitamins, minerals, amino acids, fatty acids, botanical actives, and probiotics — no partner-lab dependency, no sample-splitting delays across multiple labs.

Five regional labs

Delhi, Gurugram, Bangalore, Baddi, and Bahadurgarh — closer to your factory or warehouse means lower sample-courier risk and faster despatch.

Express service for launch deadlines

Time-critical claim panels available on express turnaround for marketplace launches, FSSAI deadlines, and surveillance response windows.

Frequently Asked Questions

What is label claims verification for nutraceuticals?
Label claims verification is the analytical confirmation that the active ingredient content declared on the label of a health supplement, dietary supplement, or functional food is present at or above the claimed quantity in the finished product. Under FSSAI Health Supplements Regulations 2016, every nutrient or active claimed on the label must be quantified and substantiated. Auriga validates vitamins, minerals, amino acids, omega fatty acids, botanical actives, probiotics, and other declared nutrients against the printed label values using validated HPLC, GC-FID, ICP-MS, LC-MS/MS, and microbiological assay methods.
What tolerance does FSSAI allow on label-claimed nutrient values?
For nutrients claimed on the label as added (e.g., "contains 500 mg vitamin C"), FSSAI requires the analytical value to be at least 80% of the declared value through the product's shelf life. For nutrients restricted by claim (e.g., "low sodium"), the value must not exceed the declared figure. The general ±20% tolerance applies to the nutrition information panel, but claim-bearing nutrients carry the stricter 80% floor. Practical guidance: build an overage into your formulation so the analytical value comfortably exceeds the label claim at end of shelf life.
Which analytical methods are used for nutrient quantification?
HPLC for water-soluble vitamins (B-complex, C) and fat-soluble vitamins (A, D, E, K); microbiological assay for B12 and folic acid where HPLC sensitivity is insufficient; ICP-OES / ICP-MS for minerals (Ca, Fe, Zn, Mg, K, Cu, Se, Cr); GC-FID for omega-3 / omega-6 fatty acid profiles (EPA, DHA, ALA); HPLC and amino acid analyser for amino acids (BCAAs, glutamine, arginine, taurine); HPLC-UV / LC-MS for botanical actives (curcuminoids, withanolides, ginsenosides, gymnemic acid).
How long does label claims verification take?
A single-claim panel (e.g., vitamin C only) takes 5–7 working days. A typical multi-vitamin / multi-mineral panel of 10–18 claims takes 10–14 working days. Complex panels combining vitamins + minerals + amino acids + probiotic counts can take 14–18 working days. Express service at 7 working days is available for FSSAI registration submissions and marketplace listing deadlines.
What sample quantity is required for label claims verification?
Send at least 60 g of finished product or 60 tablets/capsules in sealed retail packaging — the quantity scales with the breadth of the claim panel. For probiotic claim verification, dispatch additional sample under cold-chain conditions (2–8 °C). For products with multiple flavours, variants, or pack sizes, send representative samples from each. Our SPOC will confirm the exact quantity for your specific panel after reviewing the formulation and label.
What is the penalty for unverified or false label claims?
False or unsubstantiated nutritional claims are prosecuted under Section 53 of the FSS Act 2006 (Misleading Advertisement), attracting fines up to ten lakh rupees. Where the false claim renders the product misbranded under Section 52 or sub-standard under Section 51, additional penalties apply (up to five lakh rupees plus FBO licence consequences). Marketplaces automatically delist on claim failures. The CCPA can also intervene under the Consumer Protection Act for misleading commercial claims. An NABL-accredited label claims report is the primary defence document.
When should label claims be re-verified?
Re-verify label claims whenever: (a) the active-ingredient supplier changes; (b) the formulation or overage strategy changes; (c) the dosage form, packaging, or manufacturing site changes; (d) the product approaches end of shelf life and stability data suggests degradation; (e) a regulatory or marketplace challenge requires evidentiary support. As a default, annual re-verification covers most stable formulations; probiotic and live-microorganism claims need more frequent verification through shelf life.

Get Your Label Claims Verification Quote

NABL-accredited verification of vitamins, minerals, amino acids, omegas, and botanicals against label values. FSSAI 2016 compliance with label-ready output.

Call Now Get a Quote

Type to search services, tests, and locations…