NDC 21839-570 Coola Refreshing Water Mist Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 21839-570?
What are the uses for Coola Refreshing Water Mist Sunscreen Spf 30?
Which are Coola Refreshing Water Mist Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Coola Refreshing Water Mist Sunscreen Spf 30 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:
- WATER (UNII: 059QF0KO0R)
- JASMINUM SAMBAC FLOWER (UNII: 2S686I937F)
- SOYBEAN (UNII: L7HT8F1ZOD)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- ALCOHOL (UNII: 3K9958V90M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- TROPOLONE (UNII: 7L6DL16P1T)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- COCOA (UNII: D9108TZ9KG)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- SCHINUS MOLLE FRUITING TOP (UNII: T8L6O1KSB4)
- ETHYL OLIVATE (UNII: KKJ108Y20W)
- COCONUT WATER (UNII: 267F5Y81NT)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PROPANEDIOL (UNII: 5965N8W85T)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
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[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".