NDC 42248-122 Sun Care For Body
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 42248-122?
Which are Sun Care For Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Sun Care For Body 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W)
- PEG-8 STEARATE (UNII: 2P9L47VI5E)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 900 KD) (UNII: B70CUU14M9)
- WATER (UNII: 059QF0KO0R)
- TRICAPRYLIN (UNII: 6P92858988)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- C12-14 ISOPARAFFIN (UNII: WP37Z9V66A)
- 1-ETHYL-2-PYRROLECARBOXALDEHYDE (UNII: 51J1CE738Y)
- RICE GERM (UNII: 7N2B70SFEZ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- LAURETH-7 (UNII: Z95S6G8201)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ALLANTOIN (UNII: 344S277G0Z)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALCOHOL (UNII: 3K9958V90M)
- PEG-32 STEARATE (UNII: 33GX5WQC0M)
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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".