dandruff
Generic: pyrithione zinc
Labeler: valu merchandisers companyDrug Facts
Product Profile
Brand Name
dandruff
Generic Name
pyrithione zinc
Labeler
valu merchandisers company
Dosage Form
SHAMPOO
Routes
Active Ingredients
pyrithione zinc 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63941-311
Product ID
63941-311_4af5faa0-1356-7489-e063-6294a90aae4e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M032
Listing Expiration
2027-12-31
Marketing Start
2009-01-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63941311
Hyphenated Format
63941-311
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 370 mL in 1 BOTTLE, PLASTIC (63941-311-32)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4af5faa0-1356-7489-e063-6294a90aae4e", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["d5dd333d-fea5-4e03-bd9f-cbc28ea48a80"], "manufacturer_name": ["Valu Merchandisers Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "370 mL in 1 BOTTLE, PLASTIC (63941-311-32)", "package_ndc": "63941-311-32", "marketing_start_date": "20231115"}], "brand_name": "Dandruff", "product_id": "63941-311_4af5faa0-1356-7489-e063-6294a90aae4e", "dosage_form": "SHAMPOO", "product_ndc": "63941-311", "generic_name": "Pyrithione zinc", "labeler_name": "Valu Merchandisers Company", "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": "20090106", "listing_expiration_date": "20271231"}