NDC 13630-0110 Australian Gold Botanical Sunscreen Broad Spectrum Spf 30 Natural
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13630 - Prime Packaging Inc.
- 13630-0110 - Australian Gold
Product Characteristics
Product Packages
NDC Code 13630-0110-4
Package Description: 177 mL in 1 CAN
Product Details
What is NDC 13630-0110?
What are the uses for Australian Gold Botanical Sunscreen Broad Spectrum Spf 30 Natural?
Which are Australian Gold Botanical Sunscreen Broad Spectrum Spf 30 Natural UNII Codes?
The UNII codes for the active ingredients in this product are:
- 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 Botanical Sunscreen Broad Spectrum Spf 30 Natural 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:
- BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)
- ALCOHOL (UNII: 3K9958V90M)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
- KAKADU PLUM (UNII: 0ZQ1D2FDLI)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- GLYCERIN (UNII: PDC6A3C0OX)
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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".