NDC 70281-208 Op Protect And Nourish Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70281 - Solskyn Personal Care Llc
- 70281-208 - Op Protect And Nourish Spf 30 Sunscreen
Product Packages
NDC Code 70281-208-04
Package Description: 89 g in 1 CONTAINER
Product Details
What is NDC 70281-208?
What are the uses for Op Protect And Nourish Spf 30 Sunscreen?
Which are Op Protect And Nourish Spf 30 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)
Which are Op Protect And Nourish Spf 30 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)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- 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".