NDC 59970-080 Cold And Hot Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59970 - Navarro Discount Pharmacies,llc
- 59970-080 - Cold And Hot Pain Relief
Product Packages
NDC Code 59970-080-05
Package Description: 1 POUCH in 1 CARTON / 5 PATCH in 1 POUCH
Product Details
What is NDC 59970-080?
What are the uses for Cold And Hot Pain Relief?
Which are Cold And Hot Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Cold And Hot Pain Relief 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:
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- TARTARIC ACID (UNII: W4888I119H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Cold And Hot Pain Relief?
- RxCUI: 420222 - menthol 5 % Medicated Patch
- RxCUI: 420222 - menthol 0.05 MG/MG Medicated Patch
* 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".