NDC 0363-0864 Walgreens Cold Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 0363-0864?
What are the uses for Walgreens Cold Pain Relief?
Which are Walgreens Cold Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Walgreens Cold Pain Relief 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)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- GLYCERIN (UNII: PDC6A3C0OX)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Walgreens Cold Pain Relief?
- RxCUI: 415974 - menthol 4 % Topical Gel
- RxCUI: 415974 - menthol 0.04 MG/MG Topical Gel
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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".