NDC 81757-002 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81757 - Imperfect Foods
- 81757-002 - Sunscreen
Product Packages
NDC Code 81757-002-06
Package Description: 171 g in 1 CAN
Product Details
What is NDC 81757-002?
What are the uses for Sunscreen?
Which are Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENTONITE (UNII: A3N5ZCN45C)
- .BETA.-BISABOLOL (UNII: LP618AV2EA)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- .ALPHA.-CELLULOSE (UNII: I355QGZ19A)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- COCO GLUCOSIDE (UNII: ICS790225B)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER SEED OIL GLYCERETH-8 ESTERS (UNII: 358X17CAT0)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- 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".