NDC 49035-025 Equate Purifying Cleanser
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49035 - Wal-mart Stores Inc
- 49035-025 - Equate Purifying Cleanser
Product Packages
NDC Code 49035-025-70
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 120 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 49035-025?
What are the uses for Equate Purifying Cleanser?
Which are Equate Purifying Cleanser UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Equate Purifying Cleanser 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)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
- SORBITOL (UNII: 506T60A25R)
- DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
- TRIDECYL STEARATE (UNII: A8OE252M6L)
- NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K)
- LOW DENSITY POLYETHYLENE (UNII: J245LN42AI)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- CHAMOMILE (UNII: FGL3685T2X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- XANTHAN GUM (UNII: TTV12P4NEE)
- IMIDUREA (UNII: M629807ATL)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Equate Purifying Cleanser?
- RxCUI: 845836 - benzoyl peroxide 2.5 % Medicated Liquid Soap
- RxCUI: 845836 - benzoyl peroxide 25 MG/ML Medicated Liquid Soap
* 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".