Package 10742-1301-1

Brand: oxy rapid spot treatment maximum action

Generic: benzoyl peroxide
NDC Package

Package Facts

Identity

Package NDC 10742-1301-1
Digits Only 1074213011
Product NDC 10742-1301
Product ID 10742-1301_0fa156ef-27f6-0ac8-e063-6294a90af15f
Description

1 TUBE in 1 CARTON (10742-1301-1) / 28 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2015-01-01
Brand oxy rapid spot treatment maximum action
Generic benzoyl peroxide
Sample Package No

Linked Drug Pages (1)

OXY Rapid Spot Treatment Maximum Action ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0fa156ef-27f6-0ac8-e063-6294a90af15f", "openfda": {"upc": ["0310742027068"], "unii": ["W9WZN9A0GM"], "rxcui": ["106315"], "spl_set_id": ["226dad56-e415-41ec-937a-4282c73f0d34"], "manufacturer_name": ["The Mentholatum Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (10742-1301-1)  / 28 g in 1 TUBE", "package_ndc": "10742-1301-1", "marketing_start_date": "20150101"}], "brand_name": "OXY Rapid Spot Treatment Maximum Action", "product_id": "10742-1301_0fa156ef-27f6-0ac8-e063-6294a90af15f", "dosage_form": "CREAM", "product_ndc": "10742-1301", "generic_name": "benzoyl peroxide", "labeler_name": "The Mentholatum Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OXY Rapid Spot Treatment", "brand_name_suffix": "Maximum Action", "active_ingredients": [{"name": "BENZOYL PEROXIDE", "strength": "100 mg/g"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150101", "listing_expiration_date": "20261231"}