Package 72476-951-30

Brand: sunscreen

Generic: sunscreen
NDC Package

Package Facts

Identity

Package NDC 72476-951-30
Digits Only 7247695130
Product NDC 72476-951
Product ID 72476-951_4a2cd9f2-38d7-edaf-e063-6394a90aa1c9
Description

177 mL in 1 TUBE (72476-951-30)

Marketing

Marketing Status
Marketed Since 2023-09-29
Brand sunscreen
Generic sunscreen
Sample Package No

Linked Drug Pages (1)

Sunscreen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4a2cd9f2-38d7-edaf-e063-6394a90aa1c9", "openfda": {"unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W"], "spl_set_id": ["96221c10-ebfe-4385-b6b5-d504258df36c"], "manufacturer_name": ["Retail Business Services, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 TUBE (72476-951-30)", "package_ndc": "72476-951-30", "marketing_start_date": "20230929"}], "brand_name": "Sunscreen", "product_id": "72476-951_4a2cd9f2-38d7-edaf-e063-6394a90aa1c9", "dosage_form": "LOTION", "product_ndc": "72476-951", "generic_name": "Sunscreen", "labeler_name": "Retail Business Services, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunscreen", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "120 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230929", "listing_expiration_date": "20271231"}