NDC 59279-530 Thera Rx
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59279-530?
What are the uses for Thera Rx?
Which are Thera Rx UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Thera Rx 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:
- ACETIC MONOETHANOLAMIDE (UNII: A9O0818TWD)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- BIOTIN (UNII: 6SO6U10H04)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- SARCOSINE (UNII: Z711V88R5F)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- LINOLENIC ACID (UNII: 0RBV727H71)
- MENTHOL (UNII: L7T10EIP3A)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALCOHOL (UNII: 3K9958V90M)
- JOJOBA OIL (UNII: 724GKU717M)
- SORBITOL (UNII: 506T60A25R)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- WHEAT GERM OIL (UNII: 14C97E680P)
- WATER (UNII: 059QF0KO0R)
- ZINC SULFATE (UNII: 89DS0H96TB)
What is the NDC to RxNorm Crosswalk for Thera Rx?
- RxCUI: 260054 - triclosan 0.3 % Medicated Liquid Soap
- RxCUI: 260054 - triclosan 3 MG/ML Medicated Liquid Soap
- RxCUI: 260054 - triclosan 0.3 % Foaming Medicated Hand Soap
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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".