NDC 41520-871 Careone Extra Strength Cold And Hot
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41520 - American Sales Company
- 41520-871 - Careone Extra Strength Cold And Hot
Product Packages
NDC Code 41520-871-05
Package Description: 5 PATCH in 1 CARTON / 1 PATCH in 1 PATCH
Product Details
What is NDC 41520-871?
What are the uses for Careone Extra Strength Cold And Hot?
Which are Careone Extra Strength Cold And Hot UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Careone Extra Strength Cold And 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)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CASTOR OIL (UNII: D5340Y2I9G)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- KAOLIN (UNII: 24H4NWX5CO)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- 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)
What is the NDC to RxNorm Crosswalk for Careone Extra Strength Cold And Hot?
- RxCUI: 420222 - menthol 5 % Medicated Patch
- RxCUI: 420222 - menthol 0.05 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".