NDC 72793-200 Mountain Ice Sports Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 72793-200?
What are the uses for Mountain Ice Sports Pain Relief?
Which are Mountain Ice Sports Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR OIL (UNII: 75IZZ8Y727)
- CAMPHOR OIL (UNII: 75IZZ8Y727) (Active Moiety)
Which are Mountain Ice Sports 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)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- INDIAN FRANKINCENSE OIL (UNII: 5T1XCE6K8K)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- TURMERIC OIL (UNII: 6KGS8SP16U)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ARGININE (UNII: 94ZLA3W45F)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- TEA TREE OIL (UNII: VIF565UC2G)
- SPEARMINT OIL (UNII: C3M81465G5)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Mountain Ice Sports Pain Relief?
- RxCUI: 2393535 - camphor 4 % / menthol 6 % Topical Gel
- RxCUI: 2393535 - camphor 0.04 MG/MG / menthol 0.06 MG/MG Topical Gel
* Please review the disclaimer below.
[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".