Package 68071-2307-5

Brand: benzoyl peroxide acne medication

Generic: benzoyl peroxide
NDC Package

Package Facts

Identity

Package NDC 68071-2307-5
Digits Only 6807123075
Product NDC 68071-2307
Description

42.5 mL in 1 TUBE (68071-2307-5)

Marketing

Marketing Status
Marketed Since 2020-11-30
Brand benzoyl peroxide acne medication
Generic benzoyl peroxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1d78819d-c76c-7ba4-e063-6394a90a404d", "openfda": {"upc": ["0368071230758"], "unii": ["W9WZN9A0GM"], "rxcui": ["308694"], "spl_set_id": ["b55acec6-5a4d-08b7-e053-2995a90a0f74"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "42.5 mL in 1 TUBE (68071-2307-5)", "package_ndc": "68071-2307-5", "marketing_start_date": "20201130"}], "brand_name": "Benzoyl Peroxide Acne Medication", "product_id": "68071-2307_1d78819d-c76c-7ba4-e063-6394a90a404d", "dosage_form": "GEL", "product_ndc": "68071-2307", "generic_name": "Benzoyl Peroxide", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benzoyl Peroxide", "brand_name_suffix": "Acne Medication", "active_ingredients": [{"name": "BENZOYL PEROXIDE", "strength": "50 mg/mL"}], "application_number": "M014", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150120", "listing_expiration_date": "20261231"}