NDC 11822-5648 Rite Aid Extra Strength Pain Relief Cold And Hot Medicated
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid
- 11822-5648 - Rite Aid Extra Strength Pain Relief Cold And Hot Medicated
Product Packages
NDC Code 11822-5648-1
Package Description: 1 POUCH in 1 CARTON / 3 PATCH in 1 POUCH
Product Details
What is NDC 11822-5648?
What are the uses for Rite Aid Extra Strength Pain Relief Cold And Hot Medicated?
Which are Rite Aid Extra Strength Pain Relief Cold And Hot Medicated UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Rite Aid Extra Strength Pain Relief Cold And Hot Medicated 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)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- WATER (UNII: 059QF0KO0R)
- TARTARIC ACID (UNII: W4888I119H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Rite Aid Extra Strength Pain Relief Cold And Hot Medicated?
- 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".