NDC 50544-004 Therapeutic Sulfur Mask
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50544 - University Medical Pharmaceuticals Corp
- 50544-004 - Therapeutic Sulfur Mask
Product Packages
NDC Code 50544-004-91
Package Description: 1 TUBE in 1 CARTON / 48 g in 1 TUBE (50544-004-02)
Product Details
What is NDC 50544-004?
What are the uses for Therapeutic Sulfur Mask?
Which are Therapeutic Sulfur Mask UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Therapeutic Sulfur Mask 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)
- KAOLIN (UNII: 24H4NWX5CO)
- BENTONITE (UNII: A3N5ZCN45C)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ACACIA (UNII: 5C5403N26O)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- MENTHYL LACTATE (UNII: 2BF9E65L7I)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- COPPER GLUCONATE (UNII: RV823G6G67)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- MANNITOL (UNII: 3OWL53L36A)
- EDETATE SODIUM (UNII: MP1J8420LU)
- MAGNESIUM ASPARTATE (UNII: R17X820ROL)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
What is the NDC to RxNorm Crosswalk for Therapeutic Sulfur Mask?
- RxCUI: 1098781 - sulfur 3.5 % Medicated Liquid Soap
- RxCUI: 1098781 - sulfur 35 MG/ML Medicated Liquid Soap
- RxCUI: 1098781 - sulfur 3.5 % Facial Mask
* 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".