Package 54111-174-01
Brand: nudescreen blush tint spf 30- sunset rose
Generic: zinc oxide sunscreenPackage Facts
Identity
Package NDC
54111-174-01
Digits Only
5411117401
Product NDC
54111-174
Description
1 TUBE in 1 CARTON (54111-174-01) / 15 mL in 1 TUBE
Marketing
Marketing Status
Brand
nudescreen blush tint spf 30- sunset rose
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": "f2312c7b-13f8-4622-9c6e-a3104113a830", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["e351dff2-4237-4458-a947-b894e7b670a3"], "manufacturer_name": ["Bentley Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (54111-174-01) / 15 mL in 1 TUBE", "package_ndc": "54111-174-01", "marketing_start_date": "20231227"}], "brand_name": "NUDESCREEN BLUSH TINT SPF 30- SUNSET ROSE", "product_id": "54111-174_f2312c7b-13f8-4622-9c6e-a3104113a830", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "54111-174", "generic_name": "ZINC OXIDE SUNSCREEN", "labeler_name": "Bentley Laboratories, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NUDESCREEN BLUSH TINT SPF 30- SUNSET ROSE", "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"}