NDC 49035-405 Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49035 - Wal-mart Stores Inc.
- 49035-405 - Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Product Packages
NDC Code 49035-405-06
Package Description: 177 g in 1 CONTAINER
Product Details
What is NDC 49035-405?
What are the uses for Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone?
Which are Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone 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:
- BUTYL OCTYL PHTHALATE (UNII: Y52J9Q533Y)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- EDETIC ACID (UNII: 9G34HU7RV0)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- DOCOSANOL (UNII: 9G1OE216XY)
- GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
- POLYESTER-7 (UNII: 0841698D2F)
- DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- WATER (UNII: 059QF0KO0R)
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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".