NDC 67510-0026 Medicated Pain Relief Hot
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67510 - Kareway Product, Inc.
- 67510-0026 - Medicated Pain Relief Hot
Product Packages
NDC Code 67510-0026-2
Package Description: 1 POUCH in 1 CARTON / 2 PATCH in 1 POUCH
NDC Code 67510-0026-4
Package Description: 1 POUCH in 1 CARTON / 4 PATCH in 1 POUCH
Product Details
What is NDC 67510-0026?
What are the uses for Medicated Pain Relief Hot?
Which are Medicated Pain Relief Hot UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAPSICUM OLEORESIN (UNII: UW86K581WY)
- CAPSICUM OLEORESIN (UNII: UW86K581WY) (Active Moiety)
Which are Medicated Pain Relief Hot 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- TARTARIC ACID (UNII: W4888I119H)
- GELATIN (UNII: 2G86QN327L)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Medicated Pain Relief Hot?
- RxCUI: 1191003 - capsaicin 0.002 % / menthol 0.4 % Medicated Patch
- RxCUI: 1191003 - capsaicin 0.00002 MG/MG / menthol 0.004 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".