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
SHAMPOO
Routes
Active Ingredients
pyrithione zinc 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
53942-281
Product ID
53942-281_49ef567f-c2f2-52c4-e063-6294a90a4502
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
53942281
Hyphenated Format
53942-281
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 (53942-281-32)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "49ef567f-c2f2-52c4-e063-6294a90a4502", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["584df95a-7fc7-4b4b-b703-c423248444ed"], "manufacturer_name": ["Demoulas Super Markets, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "370 mL in 1 BOTTLE, PLASTIC (53942-281-32)", "package_ndc": "53942-281-32", "marketing_start_date": "20231101"}], "brand_name": "Dandruff", "product_id": "53942-281_49ef567f-c2f2-52c4-e063-6294a90a4502", "dosage_form": "SHAMPOO", "product_ndc": "53942-281", "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"}