Package 51326-829-03

Brand: antioxidant sunscreen spf 40

Generic: octinoxate and zinc oxide
NDC Package

Package Facts

Identity

Package NDC 51326-829-03
Digits Only 5132682903
Product NDC 51326-829
Product ID 51326-829_1e23a07e-f101-477a-98ab-51df88e50464
Description

105 mL in 1 BOTTLE, PLASTIC (51326-829-03)

Marketing

Marketing Status
Marketed Since 2000-07-28
Brand antioxidant sunscreen spf 40
Generic octinoxate and zinc oxide
Sample Package No

Linked Drug Pages (1)

Antioxidant Sunscreen SPF 40 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "1e23a07e-f101-477a-98ab-51df88e50464", "openfda": {"unii": ["4Y5P7MUD51", "SOI2LOH54Z"], "spl_set_id": ["2686378c-8827-47fb-b3ed-07438bd4e9e2"], "manufacturer_name": ["Topiderm, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "105 mL in 1 BOTTLE, PLASTIC (51326-829-03)", "package_ndc": "51326-829-03", "marketing_start_date": "20000728"}], "brand_name": "Antioxidant Sunscreen SPF 40", "product_id": "51326-829_1e23a07e-f101-477a-98ab-51df88e50464", "dosage_form": "LOTION", "product_ndc": "51326-829", "generic_name": "Octinoxate and Zinc Oxide", "labeler_name": "Topiderm, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antioxidant Sunscreen SPF 40", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 mg/mL"}, {"name": "ZINC OXIDE", "strength": "70 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20000728", "listing_expiration_date": "20261231"}