NDC 45861-005 Medrox-rx
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 45861-005?
What are the uses for Medrox-rx?
Which are Medrox-rx UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Medrox-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:
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TROLAMINE (UNII: 9O3K93S3TK)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Medrox-rx?
- RxCUI: 1235753 - capsaicin 0.05 % / menthol 7 % / methyl salicylate 20 % Topical Ointment
- RxCUI: 1235753 - capsaicin 0.0005 MG/MG / menthol 0.07 MG/MG / methyl salicylate 0.2 MG/MG Topical Ointment
- RxCUI: 1235758 - Medrox-Rx 0.05 % / 7 % / 20 % Topical Ointment
- RxCUI: 1235758 - capsaicin 0.0005 MG/MG / menthol 0.07 MG/MG / methyl salicylate 0.2 MG/MG Topical Ointment [Medrox]
- RxCUI: 1235758 - Medrox-Rx (capsaicin 0.05 % / menthol 7 % / methyl salicylate 20 % ) Topical Ointment
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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".