NDC 51452-003 Cold Spot Point Relief
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51452-003?
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 CORDIFOLIA FLOWER (UNII: JCG1OSZ7A8)
- CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
- CITRIC ACID (UNII: 2968PHW8QP)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALCOHOL (UNII: 3K9958V90M)
What is the NDC to RxNorm Crosswalk for Cold Spot Point Relief?
- RxCUI: 1043283 - ColdSpot POINT RELIEF 10 % Topical Spray
- RxCUI: 1043283 - menthol 100 MG/ML Topical Spray [Cold Spot]
- RxCUI: 1043283 - Cold Spot 0.1 ML/ML Topical Spray
- RxCUI: 1043283 - Cold Spot Point Relief 10 % Topical Spray
- RxCUI: 667889 - menthol 10 % Topical Spray
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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".