Package 70707-211-15

Brand: acne med 5%

Generic: benzoyl peroxide
NDC Package

Package Facts

Identity

Package NDC 70707-211-15
Digits Only 7070721115
Product NDC 70707-211
Product ID 70707-211_0c8655bc-43b2-2b67-e063-6394a90aafa3
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (70707-211-15) / 44 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2023-01-01
Brand acne med 5%
Generic benzoyl peroxide
Sample Package No

Linked Drug Pages (1)

Acne Med 5% ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0c8655bc-43b2-2b67-e063-6394a90aafa3", "openfda": {"upc": ["0812223030142"], "unii": ["W9WZN9A0GM"], "rxcui": ["308694"], "spl_set_id": ["454983d2-4b11-6268-e054-00144ff8d46c"], "manufacturer_name": ["Face Reality, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (70707-211-15)  / 44 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "70707-211-15", "marketing_start_date": "20230101"}], "brand_name": "Acne Med 5%", "product_id": "70707-211_0c8655bc-43b2-2b67-e063-6394a90aafa3", "dosage_form": "GEL", "product_ndc": "70707-211", "generic_name": "BENZOYL PEROXIDE", "labeler_name": "Face Reality, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acne Med 5%", "active_ingredients": [{"name": "BENZOYL PEROXIDE", "strength": "50 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230101", "listing_expiration_date": "20261231"}