dandruff

Generic: pyrithione zinc

Labeler: h e b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dandruff
Generic Name pyrithione zinc
Labeler h e b
Dosage Form SHAMPOO
Routes
TOPICAL
Active Ingredients

pyrithione zinc 10 mg/mL

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-070
Product ID 37808-070_4b93c6bc-58d3-2d53-e063-6294a90ab888
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M032
Listing Expiration 2027-12-31
Marketing Start 2016-10-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808070
Hyphenated Format 37808-070

Supplemental Identifiers

RxCUI
209884
UNII
R953O2RHZ5

Packaging Origin

Original Packager
true

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
  • 370 mL in 1 BOTTLE, PLASTIC (37808-070-32)
source: ndc

Packages (1)

37808-070-32 370 mL in 1 BOTTLE, PLASTIC (37808-070-32)

Ingredients (1)

pyrithione zinc (10 mg/mL)

Linked Drug Pages (1)

Dandruff ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4b93c6bc-58d3-2d53-e063-6294a90ab888", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["0927361e-a210-4e44-bbe7-fb68b240cf4f"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "370 mL in 1 BOTTLE, PLASTIC (37808-070-32)", "package_ndc": "37808-070-32", "marketing_start_date": "20240522"}], "brand_name": "Dandruff", "product_id": "37808-070_4b93c6bc-58d3-2d53-e063-6294a90ab888", "dosage_form": "SHAMPOO", "product_ndc": "37808-070", "generic_name": "Pyrithione zinc", "labeler_name": "H E B", "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": "20161021", "listing_expiration_date": "20271231"}