NDC 50184-6500 Miracle Worker Spf 55
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50184 - Philosophy, Inc
- 50184-6500 - Miracle Worker Spf 55
Product Packages
NDC Code 50184-6500-1
Package Description: 50 mL in 1 TUBE
Product Details
What is NDC 50184-6500?
What are the uses for Miracle Worker Spf 55?
Which are Miracle Worker Spf 55 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Miracle Worker Spf 55 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HEXYLDECANOL (UNII: 151Z7P1317)
- BRASSICA RAPA VAR. RAPA (UNII: AIV6895O8B)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- WHEAT GERM (UNII: YR3G369F5A)
- GLYCERIN (UNII: PDC6A3C0OX)
- LEVOMENOL (UNII: 24WE03BX2T)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BENTONITE (UNII: A3N5ZCN45C)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TETRAPEPTIDE-21 (UNII: 179JUC43HU)
- PICEA ABIES WOOD (UNII: 72GZ8K8996)
- CETYLHYDROXYPROLINE PALMITAMIDE (UNII: 74ONU0S62G)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
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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".