NDC 81757-001 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81757 - Imperfect Foods
- 81757-001 - Sunscreen
Product Packages
NDC Code 81757-001-04
Package Description: 118 mL in 1 TUBE
Product Details
What is NDC 81757-001?
What are the uses for Sunscreen?
Which are Sunscreen 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sunscreen 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:
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- OCTAMETHYLTETRASILOXANE (UNII: YB15PH50RH)
- LAURETH-7 (UNII: Z95S6G8201)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ALLANTOIN (UNII: 344S277G0Z)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- LAUROYL LYSINE (UNII: 113171Q70B)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
* 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".