NDC 50544-001 Oil-free Acne Cleanser
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50544 - University Medical Pharmaceuticals Corp
- 50544-001 - Oil-free Acne Cleanser
Product Packages
NDC Code 50544-001-06
Package Description: 237 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 50544-001?
What are the uses for Oil-free Acne Cleanser?
Which are Oil-free Acne Cleanser UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOIC ACID (UNII: 8SKN0B0MIM) (Active Moiety)
Which are Oil-free Acne 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)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- LEVOMENOL (UNII: 24WE03BX2T)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Oil-free Acne Cleanser?
- RxCUI: 308688 - benzoyl peroxide 2.5 % Topical Cream
- RxCUI: 308688 - benzoyl peroxide 25 MG/ML Topical Cream
* 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".