NDC 0363-0149 Walgreens Medicated Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreens
- 0363-0149 - Walgreens Medicated Pain Relieving
Product Packages
NDC Code 0363-0149-40
Package Description: 2 POUCH in 1 CARTON / 20 PATCH in 1 POUCH
Product Details
What is NDC 0363-0149?
What are the uses for Walgreens Medicated Pain Relieving?
Which are Walgreens Medicated Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Walgreens Medicated Pain Relieving 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- ZINC OXIDE (UNII: SOI2LOH54Z)
What is the NDC to RxNorm Crosswalk for Walgreens Medicated Pain Relieving?
- RxCUI: 853260 - camphor 1.2 % / menthol 5.7 % / methyl salicylate 6.3 % Medicated Patch
- RxCUI: 853260 - camphor 0.012 MG/MG / menthol 0.057 MG/MG / methyl salicylate 0.063 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".