NDC 51452-004 Cold Spot Point Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 51452-004?
What are the uses for Cold Spot Point Relief?
Which are Cold Spot Point Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Cold Spot Point 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:
- WATER (UNII: 059QF0KO0R)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K)
- BROMELAINS (UNII: U182GP2CF3)
- ALCOHOL (UNII: 3K9958V90M)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
- CITRIC ACID (UNII: 2968PHW8QP)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
What is the NDC to RxNorm Crosswalk for Cold Spot Point Relief?
- RxCUI: 1191164 - menthol 12 % Medicated Pad
- RxCUI: 1191164 - menthol 120 MG/ML Medicated Pad
- RxCUI: 1191164 - menthol 12 % Medicated Wipe
- RxCUI: 1235986 - Cold Spot Point Relief 12 % Medicated Pad
- RxCUI: 1235986 - menthol 120 MG/ML Medicated Pad [Cold Spot]
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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".