NDC 69379-001 Simanix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69379 - Home Aide Diagnostics, Inc.
- 69379-001 - Simanix
Product Packages
NDC Code 69379-001-03
Package Description: 120 g in 1 BOTTLE
Product Details
What is NDC 69379-001?
What are the uses for Simanix?
Which are Simanix UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Simanix?
- RxCUI: 1656333 - capsaicin 0.0375 % / menthol 3 % / histamine dihydrochloride 0.035 % Topical Cream
- RxCUI: 1656333 - capsaicin 0.375 MG/ML / histamine dihydrochloride 0.35 MG/ML / menthol 30 MG/ML Topical Cream
- RxCUI: 1656333 - capsaicin 0.0375 % / histamine dihydrochloride 0.035 % / menthol 3 % Topical Cream
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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".