NDC 58411-367 Revive Intensite Creme Lustre Day Firming Moisture Cream Broad Spectrum Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 58411-367?
What are the uses for Revive Intensite Creme Lustre Day Firming Moisture Cream Broad Spectrum Spf 30 Sunscreen?
Which are Revive Intensite Creme Lustre Day Firming Moisture Cream Broad Spectrum Spf 30 Sunscreen 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)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Revive Intensite Creme Lustre Day Firming Moisture Cream Broad Spectrum 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:
- WATER (UNII: 059QF0KO0R)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- UNDECYLCRYLENE DIMETHICONE (10000 MW) (UNII: HA26P2LA4P)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- C13-15 ALKANE (UNII: 114P5I43UJ)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- MICA (UNII: V8A1AW0880)
- PANTHENOL (UNII: WV9CM0O67Z)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALLANTOIN (UNII: 344S277G0Z)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- CHLORELLA VULGARIS (UNII: RYQ4R60M02)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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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".