NDC 72203-015 Hydraboost Oil-free Sunscreen Spf 40
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72203 - Bluemercury
- 72203-015 - Hydraboost Oil-free Sunscreen Spf 40
Product Packages
NDC Code 72203-015-01
Package Description: 1 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE
Product Details
What is NDC 72203-015?
What are the uses for Hydraboost Oil-free Sunscreen Spf 40?
Which are Hydraboost Oil-free Sunscreen Spf 40 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Hydraboost Oil-free Sunscreen Spf 40 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)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- PROPANEDIOL (UNII: 5965N8W85T)
- ISODODECANE (UNII: A8289P68Y2)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- TRICONTANYL POVIDONE (UNII: N0SS3Q238D)
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- ALCOHOL (UNII: 3K9958V90M)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- PANTHENOL (UNII: WV9CM0O67Z)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TAMARIND JUICE (UNII: 5P6V8403U4)
- CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SORBITAN SESQUIISOSTEARATE (UNII: VU97D01BF9)
- PPG-8-CETETH-20 (UNII: MAL0SND89Q)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
* 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".