american crew
Generic: pyrithione zinc
Labeler: revlon consumer products corpDrug Facts
Product Profile
Brand Name
american crew
Generic Name
pyrithione zinc
Labeler
revlon consumer products corp
Dosage Form
SHAMPOO
Routes
Active Ingredients
pyrithione zinc 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
10967-650
Product ID
10967-650_2a843ed5-0b1e-dda7-e063-6294a90aec3c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M032
Listing Expiration
2026-12-31
Marketing Start
2013-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
10967650
Hyphenated Format
10967-650
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
american crew (source: ndc)
Generic Name
pyrithione zinc (source: ndc)
Application Number
M032 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 250 mL in 1 CONTAINER (10967-650-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2a843ed5-0b1e-dda7-e063-6294a90aec3c", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["9566b567-90be-4803-b940-e6a91750778f"], "manufacturer_name": ["Revlon Consumer Products Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 CONTAINER (10967-650-25)", "package_ndc": "10967-650-25", "marketing_start_date": "20130101"}], "brand_name": "American Crew", "product_id": "10967-650_2a843ed5-0b1e-dda7-e063-6294a90aec3c", "dosage_form": "SHAMPOO", "product_ndc": "10967-650", "generic_name": "Pyrithione Zinc", "labeler_name": "Revlon Consumer Products Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "American Crew", "active_ingredients": [{"name": "PYRITHIONE ZINC", "strength": "1 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130101", "listing_expiration_date": "20261231"}