Package 54111-190-01

Brand: 111 skin sunscreen spf 50

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 54111-190-01
Digits Only 5411119001
Product NDC 54111-190
Product ID 54111-190_3885e519-7eb8-4b06-97fe-85471b0e6951
Description

1 BOTTLE, PUMP in 1 CARTON (54111-190-01) / 50 mL in 1 BOTTLE, PUMP

Marketing

Marketing Status
Marketed Since 2025-05-23
Brand 111 skin sunscreen spf 50
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

111 SKIN SUNSCREEN SPF 50 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3885e519-7eb8-4b06-97fe-85471b0e6951", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["b1265797-71dd-4302-ab26-dbff6ccec856"], "manufacturer_name": ["Bentley Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PUMP in 1 CARTON (54111-190-01)  / 50 mL in 1 BOTTLE, PUMP", "package_ndc": "54111-190-01", "marketing_start_date": "20250523"}], "brand_name": "111 SKIN SUNSCREEN SPF 50", "product_id": "54111-190_3885e519-7eb8-4b06-97fe-85471b0e6951", "dosage_form": "SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "54111-190", "generic_name": "Zinc Oxide", "labeler_name": "Bentley Laboratories, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "111 SKIN SUNSCREEN SPF 50", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "19.5 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250523", "listing_expiration_date": "20271231"}