NDC 62802-362 Bull Frog Kids Sunscreen 35
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62802 - Sun & Skin Care Research, Llc
- 62802-362 - Bull Frog Kids Sunscreen 35
Product Packages
NDC Code 62802-362-05
Package Description: 475 g in 1 BOTTLE
Product Details
What is NDC 62802-362?
What are the uses for Bull Frog Kids Sunscreen 35?
Which are Bull Frog Kids Sunscreen 35 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Bull Frog Kids Sunscreen 35 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)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL DIMETHICONE 45 (UNII: IK315POC44)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- NYLON-12 (UNII: 446U8J075B)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- OLEA EUROPAEA FRUIT VOLATILE OIL (UNII: 8E7358CX1J)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARETH-2 (UNII: V56DFE46J5)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- STEARETH-21 (UNII: 53J3F32P58)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PVP/VA COPOLYMER (UNII: D9C330MD8B)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
* 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".