Package 84289-216-20

Brand: proski benzo

Generic: benzoyl peroxide
NDC Package

Package Facts

Identity

Package NDC 84289-216-20
Digits Only 8428921620
Product NDC 84289-216
Product ID 84289-216_30a66a1c-0afc-8695-e063-6294a90ab355
Description

1 TUBE in 1 CARTON (84289-216-20) / 20 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-04-01
Brand proski benzo
Generic benzoyl peroxide
Sample Package No

Linked Drug Pages (1)

PROSKI BENZO ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "30a66a1c-0afc-8695-e063-6294a90ab355", "openfda": {"unii": ["W9WZN9A0GM"], "rxcui": ["308694"], "spl_set_id": ["2c75b3b9-6321-dede-e063-6394a90a5880"], "manufacturer_name": ["PHARMAMED USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (84289-216-20)  / 20 g in 1 TUBE", "package_ndc": "84289-216-20", "marketing_start_date": "20250401"}], "brand_name": "PROSKI BENZO", "product_id": "84289-216_30a66a1c-0afc-8695-e063-6294a90ab355", "dosage_form": "GEL", "product_ndc": "84289-216", "generic_name": "BENZOYL PEROXIDE", "labeler_name": "PHARMAMED USA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PROSKI BENZO", "active_ingredients": [{"name": "BENZOYL PEROXIDE", "strength": "5 g/100g"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}