FSSAI files three cases against Nestlé India over infant nutrition products

FSSAI has initiated three adjudication cases against Nestlé India, citing promotional claims on NAN Excella Pro Stage 1 and Lactogen Pro 1, along with alleged non-conforming biotin levels in a follow-up formula.

— Source publishedFri, 18 Sept, 2026, 13:54 IST·First seen Fri, 18 Sept, 2026, 14:13 IST·Source Business Standard · Companies

What happened

FSSAI filed three adjudication cases against Nestle India over promotional claims on NAN Excella Pro Stage 1 and Lactogen Pro 1, plus non-conforming biotin

Key facts

  • Three infant nutrition products
  • Regulation 4(2) of the Food Safety and Standards (Foods for Infant Nutrition) Regulations, 2020
  • Section 3 of the Infant Milk Substitutes Act, 1992
  • Three separate adjudication cases
  • Nestle India shares down nearly 2% to ₹1,345.45 at 1310 hours

Why this matters

Any partnership, acquisition or portfolio review involving infant nutrition should apply heightened regulatory diligence to claims substantiation, nutrient specifications and India-specific compliance systems.

What to watch

  • FSSAI adjudication notices, hearing dates, penalties, directions to alter labels or promotions, and any recall or stop-sale order.
  • Additional FSSAI sampling results involving Nestlé products, other infant-formula brands, or other micronutrient specifications.
  • Nestlé India disclosures on provisions, product withdrawals, relabelling, sales impact or regulatory correspondence.
  • Changes in pharmacy, hospital, pediatrician and e-commerce availability of the named products.
  • Media coverage, parent-group reaction and social-media sentiment that could convert a compliance case into a trust issue.
  • Any revision or stricter enforcement guidance on infant milk substitute marketing, health claims or nutrient tolerances.
  • Conduct SKU-level audit of infant nutrition labels, digital content, medical-channel materials and retailer promotional copy.
  • Increase batch testing and supplier verification for biotin and other regulated micronutrients; document corrective-action controls.
  • Prepare a regulator-facing remediation plan and consumer communications emphasizing product safety, compliance and pediatric guidance.
  • Review inventory exposure and contingency plans for affected Stage 1 and follow-up formula products, including relabelling or withdrawal scenarios.
  • Monitor competitor claims and prepare for category-wide compliance changes that could alter promotional economics.