NDC 33992-6159 Assured Cold N Hot Pain Relief Menthol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33992 - Greenbrier International, Inc
- 33992-6159 - Assured Cold N Hot Pain Relief Menthol
Product Packages
NDC Code 33992-6159-5
Package Description: 2 POUCH in 1 PACKET / 5 mg in 1 POUCH
Product Details
What is NDC 33992-6159?
What are the uses for Assured Cold N Hot Pain Relief Menthol?
Which are Assured Cold N Hot Pain Relief Menthol UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Assured Cold N Hot Pain Relief Menthol 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- CASTOR OIL (UNII: D5340Y2I9G)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- KAOLIN (UNII: 24H4NWX5CO)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- WATER (UNII: 059QF0KO0R)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- TARTARIC ACID (UNII: W4888I119H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
What is the NDC to RxNorm Crosswalk for Assured Cold N Hot Pain Relief Menthol?
- 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".