NDC 33992-8463 Assured Extra Strength Cold N Hot
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33992 - Greenbrier International, Inc.
- 33992-8463 - Assured Extra Strength Cold N Hot
Product Packages
NDC Code 33992-8463-2
Package Description: 1 POUCH in 1 CARTON / 2 PATCH in 1 POUCH
Product Details
What is NDC 33992-8463?
What are the uses for Assured Extra Strength Cold N Hot?
Which are Assured Extra Strength Cold N Hot UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Assured Extra Strength Cold N 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GELATIN (UNII: 2G86QN327L)
- KAOLIN (UNII: 24H4NWX5CO)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- SORBITOL (UNII: 506T60A25R)
- TARTARIC ACID (UNII: W4888I119H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Assured Extra Strength Cold N Hot?
- RxCUI: 1010823 - menthol 7.5 % Medicated Patch
- RxCUI: 1010823 - menthol 0.075 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".