Package 54111-177-01
Brand: nudescreen blush tint spf 30 - sunkissed
Generic: zinc oxide sunscreenPackage Facts
Identity
Package NDC
54111-177-01
Digits Only
5411117701
Product NDC
54111-177
Description
1 TUBE in 1 CARTON (54111-177-01) / 15 mL in 1 TUBE
Marketing
Marketing Status
Brand
nudescreen blush tint spf 30 - sunkissed
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": "5e4577c0-4bc9-4f0f-a15f-f6569457559e", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["c45b59d8-0196-4dce-bfaa-57c47f655fe8"], "manufacturer_name": ["Bentley Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (54111-177-01) / 15 mL in 1 TUBE", "package_ndc": "54111-177-01", "marketing_start_date": "20231227"}], "brand_name": "NUDESCREEN BLUSH TINT SPF 30 - SUNKISSED", "product_id": "54111-177_5e4577c0-4bc9-4f0f-a15f-f6569457559e", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "54111-177", "generic_name": "ZINC OXIDE SUNSCREEN", "labeler_name": "Bentley Laboratories, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NUDESCREEN BLUSH TINT SPF 30 - SUNKISSED", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "15 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231227", "listing_expiration_date": "20261231"}