NDC 30142-928 Kroger Baby Sunscreen Spf 70
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 30142-928?
What are the uses for Kroger Baby Sunscreen Spf 70?
Which are Kroger Baby Sunscreen Spf 70 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Kroger Baby Sunscreen Spf 70 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)
- DOCOSANOL (UNII: 9G1OE216XY)
- PALMITIC ACID (UNII: 2V16EO95H1)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- LAURYL ALCOHOL (UNII: 178A96NLP2)
- MYRISTYL ALCOHOL (UNII: V42034O9PU)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- TRICAPRIN (UNII: O1PB8EU98M)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- TOCOPHEROL (UNII: R0ZB2556P8)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
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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".