NDC 13630-0019 Australian Gold Broad Spectrum Spf 4
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13630 - Prime Packaging, Inc.
- 13630-0019 - Australian Gold
Product Characteristics
Product Packages
NDC Code 13630-0019-4
Package Description: 177 mL in 1 CAN
Product Details
What is NDC 13630-0019?
What are the uses for Australian Gold Broad Spectrum Spf 4?
Which are Australian Gold Broad Spectrum Spf 4 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 4 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:
- ALCOHOL (UNII: 3K9958V90M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
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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".