NDC 68258-3984 Medrox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68258 - Dispensing Solutions, Inc.
- 68258-3984 - Medrox
Product Packages
NDC Code 68258-3984-4
Package Description: 120 g in 1 BOTTLE
Product Details
What is NDC 68258-3984?
What are the uses for Medrox?
Which are Medrox UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Medrox 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)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- TROLAMINE (UNII: 9O3K93S3TK)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Medrox?
- RxCUI: 2001749 - capsaicin 0.0375 % / menthol 5 % / methyl salicylate 20 % Topical Ointment
- RxCUI: 2001749 - capsaicin 0.000375 MG/MG / menthol 0.05 MG/MG / methyl salicylate 0.2 MG/MG Topical Ointment
- RxCUI: 2001750 - Medrox 0.038 % / 5 % / 20 % Topical Ointment
- RxCUI: 2001750 - capsaicin 0.000375 MG/MG / menthol 0.05 MG/MG / methyl salicylate 0.2 MG/MG Topical Ointment [Medrox]
- RxCUI: 2001750 - Medrox (capsaicin 0.000375 MG/MG / menthol 0.05 MG/MG / methyl salicylate 0.2 MG/MG) Topical Ointment
* 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".