NDC 58443-0280 Australian Gold Instant Bronzer 15 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58443-0280?
What are the uses for Australian Gold Instant Bronzer 15 Sunscreen?
Which are Australian Gold Instant Bronzer 15 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Australian Gold Instant Bronzer 15 Sunscreen Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- KAKADU PLUM (UNII: 0ZQ1D2FDLI)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- ALLANTOIN (UNII: 344S277G0Z)
- TEA TREE OIL (UNII: VIF565UC2G)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- CARAMEL (UNII: T9D99G2B1R)
- CARBOMER 980 (UNII: 4Q93RCW27E)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- WATER (UNII: 059QF0KO0R)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- COCOA BUTTER (UNII: 512OYT1CRR)
- ISOPROPYLPHTHALIMIDE (UNII: 1J1MM83329)
- N-BUTYLPHTHALIMIDE (UNII: 5TH1DKT35E)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".