NDC 70281-123 No-ad Sport 50 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70281 - Solskyn Personal Care Llc
- 70281-123 - No-ad Sport 50 Sunscreen
Product Packages
NDC Code 70281-123-44
Package Description: 475 g in 1 BOTTLE
Product Details
What is NDC 70281-123?
What are the uses for No-ad Sport 50 Sunscreen?
Which are No-ad Sport 50 Sunscreen 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 No-ad Sport 50 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:
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- ACETATE ION (UNII: 569DQM74SC)
- TROLAMINE (UNII: 9O3K93S3TK)
- 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".