NDC 71804-250 Mdacne Customized Cream (benzoyl Peroxide)
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What is NDC 71804-250?
What are the uses for Mdacne Customized Cream (benzoyl Peroxide)?
Which are Mdacne Customized Cream (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 Mdacne Customized Cream (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)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CUCUMBER (UNII: YY7C30VXJT)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-20 (UNII: L0Q8IK9E08)
- EDETATE SODIUM (UNII: MP1J8420LU)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- CORN (UNII: 0N8672707O)
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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".