NDC 58443-0029 Australian Gold Broad Spectrum Spf 8
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises, Inc.
- 58443-0029 - Australian Gold
Product Characteristics
Product Packages
NDC Code 58443-0029-4
Package Description: 177 mL in 1 TUBE
Product Details
What is NDC 58443-0029?
What are the uses for Australian Gold Broad Spectrum Spf 8?
Which are Australian Gold Broad Spectrum Spf 8 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 8 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:
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- 3-BUTYLPHTHALIDE (UNII: 822Q956KGM)
- ISOPROPYLPHTHALIMIDE (UNII: 1J1MM83329)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- GLYCYRRHIZA GLABRA LEAF (UNII: GH32M797Y9)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- STYRENE (UNII: 44LJ2U959V)
* 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".