NDC 49035-021 Benzoyl Peroxide
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49035-021?
What are the uses for Benzoyl Peroxide?
Which are Benzoyl Peroxide 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 Benzoyl Peroxide 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)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- PEG-12 STEARATE (UNII: 9KU38O8CEK)
- SORBITOL (UNII: 506T60A25R)
- DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
- TRIDECYL STEARATE (UNII: A8OE252M6L)
- NEOPENTYL GLYCOL (UNII: QI80HXD6S5)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- XANTHAN GUM (UNII: TTV12P4NEE)
- IMIDUREA (UNII: M629807ATL)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALLANTOIN (UNII: 344S277G0Z)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Benzoyl Peroxide?
- RxCUI: 200009 - benzoyl peroxide 2.5 % Topical Lotion
- RxCUI: 200009 - benzoyl peroxide 25 MG/ML Topical Lotion
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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".