Package 71501-1904-1

Brand: dr loretta universal glow daily defense spf 40

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 71501-1904-1
Digits Only 7150119041
Product NDC 71501-1904
Product ID 71501-1904_2de40ee1-ec9e-a4fc-e063-6294a90a7cb1
Description

50 mL in 1 TUBE, WITH APPLICATOR (71501-1904-1)

Marketing

Marketing Status
Marketed Since 2025-02-05
Brand dr loretta universal glow daily defense spf 40
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Dr Loretta Universal Glow Daily Defense SPF 40 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2de40ee1-ec9e-a4fc-e063-6294a90a7cb1", "openfda": {"upc": ["0185854000434"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["ebdaf6c1-1572-4840-851b-6d780471fcb2"], "manufacturer_name": ["Dr. Loretta, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 TUBE, WITH APPLICATOR (71501-1904-1)", "package_ndc": "71501-1904-1", "marketing_start_date": "20250205"}], "brand_name": "Dr Loretta Universal Glow Daily Defense SPF 40", "product_id": "71501-1904_2de40ee1-ec9e-a4fc-e063-6294a90a7cb1", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "71501-1904", "generic_name": "ZINC OXIDE", "labeler_name": "Dr. Loretta, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dr Loretta Universal Glow Daily Defense SPF 40", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "170 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250205", "listing_expiration_date": "20261231"}