NDC 58443-0081 Australian Gold Broad Spectrum Spf30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises, Inc.
- 58443-0081 - Australian Gold
Product Characteristics
Product Packages
NDC Code 58443-0081-4
Package Description: 150 mL in 1 BOTTLE
Product Details
What is NDC 58443-0081?
What are the uses for Australian Gold Broad Spectrum Spf30?
Which are Australian Gold Broad Spectrum Spf30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Australian Gold Broad Spectrum Spf30 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:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIBUTYL ADIPATE (UNII: F4K100DXP3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUDDLEJA DAVIDII LEAF (UNII: X380815D32)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- XANTHAN GUM (UNII: TTV12P4NEE)
* 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".