NDC 13630-0236 Australian Gold Spf 6 Bronzer Oxybenzone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13630 - Prime Packaging, Inc.
- 13630-0236 - Australian Gold
Product Characteristics
Product Packages
NDC Code 13630-0236-4
Package Description: 237 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 13630-0236?
What are the uses for Australian Gold Spf 6 Bronzer Oxybenzone?
Which are Australian Gold Spf 6 Bronzer Oxybenzone 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)
Which are Australian Gold Spf 6 Bronzer Oxybenzone 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:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- TEA TREE OIL (UNII: VIF565UC2G)
- KAKADU PLUM (UNII: 0ZQ1D2FDLI)
- N-BUTYLPHTHALIMIDE (UNII: 5TH1DKT35E)
- CARAMEL (UNII: T9D99G2B1R)
- ISOPROPYLPHTHALIMIDE (UNII: 1J1MM83329)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
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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".