NDC 36800-870 Baby Gentle Sunscreen Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 36800-870?
What are the uses for Baby Gentle Sunscreen Spf 50?
Which are Baby Gentle Sunscreen Spf 50 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 Baby Gentle Sunscreen Spf 50 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:
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- SORBITOL (UNII: 506T60A25R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TROLAMINE (UNII: 9O3K93S3TK)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- WATER (UNII: 059QF0KO0R)
* Please review the disclaimer below.
[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".