Package 46007-204-11
Brand: skinsuit face spf 50
Generic: zinc oxidePackage Facts
Identity
Package NDC
46007-204-11
Digits Only
4600720411
Product NDC
46007-204
Description
50 mL in 1 TUBE (46007-204-11)
Marketing
Marketing Status
Brand
skinsuit face spf 50
Generic
zinc oxide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2b39ef60-16c3-f252-e063-6394a90ae402", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["389fc528-fda5-485a-ab37-f99fcf3ed0b3"], "manufacturer_name": ["Skin Authority LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 TUBE (46007-204-11)", "package_ndc": "46007-204-11", "marketing_start_date": "20200102"}], "brand_name": "SKINSUIT FACE SPF 50", "product_id": "46007-204_2b39ef60-16c3-f252-e063-6394a90ae402", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "46007-204", "generic_name": "ZINC OXIDE", "labeler_name": "Skin Authority LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SKINSUIT FACE", "brand_name_suffix": "SPF 50", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "12 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120419", "listing_expiration_date": "20261231"}