NDC 71804-400 Mdacne Customized Cream (sulfur)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71804 - Mdalgorithms Inc.
- 71804-400 - Mdacne Customized Cream (sulfur)
Product Packages
NDC Code 71804-400-01
Package Description: 15 mL in 1 TUBE
Product Details
What is NDC 71804-400?
What are the uses for Mdacne Customized Cream (sulfur)?
Which are Mdacne Customized Cream (sulfur) UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Mdacne Customized Cream (sulfur) 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)
- AZELAIC ACID (UNII: F2VW3D43YT)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHAMOMILE (UNII: FGL3685T2X)
- CUCUMBER (UNII: YY7C30VXJT)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- WITCH HAZEL (UNII: 101I4J0U34)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- NIACINAMIDE (UNII: 25X51I8RD4)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-20 (UNII: L0Q8IK9E08)
- EDETATE SODIUM (UNII: MP1J8420LU)
- THYME (UNII: CW657OBU4N)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- CORN (UNII: 0N8672707O)
What is the NDC to RxNorm Crosswalk for Mdacne Customized Cream (sulfur)?
- RxCUI: 199632 - sulfur 3 % Topical Cream
- RxCUI: 199632 - sulfur 30 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".