Package 76162-362-32

Brand: 2 in 1 dandruff

Generic: pyrithione zinc
NDC Package

Package Facts

Identity

Package NDC 76162-362-32
Digits Only 7616236232
Product NDC 76162-362
Description

370 mL in 1 BOTTLE, PLASTIC (76162-362-32)

Marketing

Marketing Status
Marketed Since 2024-10-28
Brand 2 in 1 dandruff
Generic pyrithione zinc
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4ab941eb-7501-fd07-e063-6394a90ac812", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["7da1e057-a69e-4b89-a309-919d88da3b93"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "370 mL in 1 BOTTLE, PLASTIC (76162-362-32)", "package_ndc": "76162-362-32", "marketing_start_date": "20241028"}], "brand_name": "2 in 1 Dandruff", "product_id": "76162-362_4ab941eb-7501-fd07-e063-6394a90ac812", "dosage_form": "SHAMPOO", "product_ndc": "76162-362", "generic_name": "Pyrithione zinc", "labeler_name": "Topco Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "2 in 1 Dandruff", "active_ingredients": [{"name": "PYRITHIONE ZINC", "strength": "10 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241028", "listing_expiration_date": "20271231"}