NDC 11822-9006 Rite Aid Dark Tanning Spf 4
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 11822-9006?
What are the uses for Rite Aid Dark Tanning Spf 4?
Which are Rite Aid Dark Tanning Spf 4 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Rite Aid Dark Tanning 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:
- WATER (UNII: 059QF0KO0R)
- PETROLATUM (UNII: 4T6H12BN9U)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- TROLAMINE (UNII: 9O3K93S3TK)
- PEG-100 STEARATE (UNII: YD01N1999R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- COCOA BUTTER (UNII: 512OYT1CRR)
- SHEA BUTTER (UNII: K49155WL9Y)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- QUATERNIUM-15 (UNII: E40U03LEM0)
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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".