dandruff
Generic: pyrithione zinc
Labeler: demoulas super markets, incDrug Facts
Product Profile
Brand Name
dandruff
Generic Name
pyrithione zinc
Labeler
demoulas super markets, inc
Dosage Form
LOTION/SHAMPOO
Routes
Active Ingredients
pyrithione zinc 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
53942-311
Product ID
53942-311_49ef6910-c576-0379-e063-6394a90ab0d2
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M032
Listing Expiration
2027-12-31
Marketing Start
2009-01-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53942311
Hyphenated Format
53942-311
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 (53942-311-32)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "49ef6910-c576-0379-e063-6394a90ab0d2", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["6515b35c-49cb-41b4-9eb5-46dee482079e"], "manufacturer_name": ["Demoulas Super Markets, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "370 mL in 1 BOTTLE, PLASTIC (53942-311-32)", "package_ndc": "53942-311-32", "marketing_start_date": "20231102"}], "brand_name": "Dandruff", "product_id": "53942-311_49ef6910-c576-0379-e063-6394a90ab0d2", "dosage_form": "LOTION/SHAMPOO", "product_ndc": "53942-311", "generic_name": "PYRITHIONE ZINC", "labeler_name": "Demoulas Super Markets, 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": "20090130", "listing_expiration_date": "20271231"}