NDC 77462-009 Bebak Baby Sun
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 77462-009?
What are the uses for Bebak Baby Sun?
Which are Bebak Baby Sun UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Bebak Baby Sun 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:
- FRUCTOSE (UNII: 6YSS42VSEV)
- TROLAMINE (UNII: 9O3K93S3TK)
- AVOBENZONE (UNII: G63QQF2NOX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM ACETATE (UNII: 4550K0SC9B)
- CARROT (UNII: L56Z1JK48B)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- HOMOSALATE (UNII: V06SV4M95S)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- .BETA.-CAROTENE (UNII: 01YAE03M7J)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- INULIN (UNII: JOS53KRJ01)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
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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".