Dandruff

Generic: Pyrithione Zinc

Labeler: Walmart Inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Active

Drug Facts

Product Profile

Brand Name Dandruff
Generic Name Pyrithione Zinc
Labeler Walmart Inc.
Dosage Form SHAMPOO
Routes
TOPICAL
Active Ingredients

PYRITHIONE ZINC 10 mg/mL

Identifiers & Regulatory

Product NDC 79903-332
Product ID 79903-332_2f853d45-0299-a14e-e063-6394a90a123c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M032
Listing Expiration 2026-12-31
Marketing Start 2025-03-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 79903332
Hyphenated Format 79903-332

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name Dandruff (source: ndc)
Generic Name Pyrithione Zinc (source: ndc)
Application Number M032 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 834 mL in 1 BOTTLE, PLASTIC (79903-332-01)
source: ndc

Packages (1)

Ingredients (1)

PYRITHIONE ZINC (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2f853d45-0299-a14e-e063-6394a90a123c", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["e4fd5d8b-a916-41c3-b05e-a32dd528f00f"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "834 mL in 1 BOTTLE, PLASTIC (79903-332-01)", "package_ndc": "79903-332-01", "marketing_start_date": "20250304"}], "brand_name": "Dandruff", "product_id": "79903-332_2f853d45-0299-a14e-e063-6394a90a123c", "dosage_form": "SHAMPOO", "product_ndc": "79903-332", "generic_name": "Pyrithione Zinc", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dandruff", "active_ingredients": [{"name": "PYRITHIONE ZINC", "strength": "10 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250304", "listing_expiration_date": "20261231"}