NDC 58443-0220 Australian Gold Broad Spectrum Spf 4 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 58443-0220?
What are the uses for Australian Gold Broad Spectrum Spf 4 Sunscreen?
Which are Australian Gold Broad Spectrum Spf 4 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Australian Gold Broad Spectrum Spf 4 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:
- TEA TREE OIL (UNII: VIF565UC2G)
- COCOA BUTTER (UNII: 512OYT1CRR)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- KAKADU PLUM (UNII: 0ZQ1D2FDLI)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALLANTOIN (UNII: 344S277G0Z)
- WATER (UNII: 059QF0KO0R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- N-BUTYLPHTHALIMIDE (UNII: 5TH1DKT35E)
- TROLAMINE (UNII: 9O3K93S3TK)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- ISOPROPYLPHTHALIMIDE (UNII: 1J1MM83329)
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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".