Dry Scalp Dandruff

Generic: Pyrithione Zinc

Labeler: HEB
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Active

Drug Facts

Product Profile

Brand Name Dry Scalp Dandruff
Generic Name Pyrithione Zinc
Labeler HEB
Dosage Form SHAMPOO
Routes
TOPICAL
Active Ingredients

PYRITHIONE ZINC 10 mg/mL

Identifiers & Regulatory

Product NDC 37808-281
Product ID 37808-281_48c078c8-eb41-84f4-e063-6394a90a8699
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M032
Listing Expiration 2027-12-31
Marketing Start 2016-10-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808281
Hyphenated Format 37808-281

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 Dry Scalp 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
  • 370 mL in 1 BOTTLE, PLASTIC (37808-281-32)
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": "48c078c8-eb41-84f4-e063-6394a90a8699", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["626933cb-9c84-4f37-943c-2a9bd21fcea5"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "370 mL in 1 BOTTLE, PLASTIC (37808-281-32)", "package_ndc": "37808-281-32", "marketing_start_date": "20240523"}], "brand_name": "Dry Scalp Dandruff", "product_id": "37808-281_48c078c8-eb41-84f4-e063-6394a90a8699", "dosage_form": "SHAMPOO", "product_ndc": "37808-281", "generic_name": "Pyrithione Zinc", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dry Scalp Dandruff", "active_ingredients": [{"name": "PYRITHIONE ZINC", "strength": "10 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20161026", "listing_expiration_date": "20271231"}