NDC 58443-0199 Australian Gold Broad Spectrum Spf 50 X-treme Sport Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises Inc.
- 58443-0199 - Australian Gold
Product Characteristics
Product Packages
NDC Code 58443-0199-4
Package Description: 237 mL in 1 BOTTLE
Product Details
What is NDC 58443-0199?
What are the uses for Australian Gold Broad Spectrum Spf 50 X-treme Sport Sunscreen?
Which are Australian Gold Broad Spectrum Spf 50 X-treme Sport Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Australian Gold Broad Spectrum Spf 50 X-treme Sport 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)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- ISOPROPYLPHTHALIMIDE (UNII: 1J1MM83329)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- N-BUTYLPHTHALIMIDE (UNII: 5TH1DKT35E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- KAKADU PLUM (UNII: 0ZQ1D2FDLI)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
* Please review the disclaimer below.
[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".