NDC 21839-452 Coola Classic Face Sunscreen Fragrance-free Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21839 - Gordon Laboratories, Inc.
- 21839-452 - Coola Classic Face Sunscreen Fragrance-free
Product Packages
NDC Code 21839-452-02
Package Description: 1 TUBE in 1 CARTON / 148 mL in 1 TUBE (21839-452-01)
Product Details
What is NDC 21839-452?
What are the uses for Coola Classic Face Sunscreen Fragrance-free Spf 50?
Which are Coola Classic Face Sunscreen Fragrance-free Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Coola Classic Face Sunscreen Fragrance-free Spf 50 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:
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- WATER (UNII: 059QF0KO0R)
- TROPOLONE (UNII: 7L6DL16P1T)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALCOHOL (UNII: 3K9958V90M)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
- OPUNTIA FICUS-INDICA (UNII: 23Z87HTQ6P)
- JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- CARTHAMUS TINCTORIUS SEEDCAKE (UNII: DHQ13F4N2W)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MAURITIA FLEXUOSA FRUIT OIL (UNII: 48H19MS04L)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- GLYCERIN (UNII: PDC6A3C0OX)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CAMELINA SATIVA SEED OIL (UNII: 12824X01L0)
- CANOLA OIL (UNII: 331KBJ17RK)
* 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".