NDC 49035-300 Equate Beauty Road Spectrum Spf30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49035 - Wal-mart Stores, Inc
- 49035-300 - Equate Beauty
Product Packages
NDC Code 49035-300-16
Package Description: 1 BOTTLE in 1 CARTON / 29 g in 1 BOTTLE
Product Details
What is NDC 49035-300?
What are the uses for Equate Beauty Road Spectrum Spf30?
Which are Equate Beauty Road Spectrum Spf30 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)
Which are Equate Beauty Road Spectrum Spf30 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRISILOXANE (UNII: 9G1ZW13R0G)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARETH-21 (UNII: 53J3F32P58)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- STYRENE (UNII: 44LJ2U959V)
- SODIUM (UNII: 9NEZ333N27)
- DIVINYLBENZENE (UNII: IZ715T4SBU)
- AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MYRTUS COMMUNIS LEAF (UNII: U20N87188F)
- XANTHAN GUM (UNII: TTV12P4NEE)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALLYL ACRYLATE (UNII: 705GA5O3US)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TRIS-BHT MESITYLENE (UNII: 51DM34B894)
- HYALURONIC ACID (UNII: S270N0TRQY)
* 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".