NDC 69379-285 Remaxazon External Patch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69379 - Home Aide Diagnostics, Inc.
- 69379-285 - Remaxazon External Patch
Product Packages
NDC Code 69379-285-15
Package Description: 5 PACKAGE in 1 BOX / 3 PATCH in 1 PACKAGE / 100 g in 1 PATCH
Product Details
What is NDC 69379-285?
Which are Remaxazon External Patch UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHONDROITIN SULFATE SODIUM (BOVINE) (UNII: 8QTV3DTT8W)
- CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- GLUCOSAMINE (UNII: N08U5BOQ1K)
- GLUCOSAMINE (UNII: N08U5BOQ1K) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Remaxazon External Patch?
- RxCUI: 1605123 - capsaicin 0.0285 % / chondroitin sulfates 3 % / glucosamine 5 % / lidocaine 4 % Medicated Patch
- RxCUI: 1605123 - capsaicin 0.000285 MG/MG / chondroitin sulfates 0.03 MG/MG / glucosamine 0.05 MG/MG / lidocaine 0.04 MG/MG Medicated Patch
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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".