Package 54111-183-01

Brand: mineral sunscreen

Generic: zinc oxide sunscreen
NDC Package

Package Facts

Identity

Package NDC 54111-183-01
Digits Only 5411118301
Product NDC 54111-183
Description

1 TUBE in 1 CARTON (54111-183-01) / 42 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2020-12-15
Brand mineral sunscreen
Generic zinc oxide sunscreen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "8fbbcad3-e255-4f2a-9902-00f6316a253c", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["782a8641-7e6a-413b-a2ed-0efeb36c48a7"], "manufacturer_name": ["Bentley Laboratories LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (54111-183-01)  / 42 mL in 1 TUBE", "package_ndc": "54111-183-01", "marketing_start_date": "20201215"}], "brand_name": "Mineral Sunscreen", "product_id": "54111-183_8fbbcad3-e255-4f2a-9902-00f6316a253c", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "54111-183", "generic_name": "Zinc Oxide Sunscreen", "labeler_name": "Bentley Laboratories LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mineral Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "12.025 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201215", "listing_expiration_date": "20261231"}