NDC 61995-0602 Jason Cooling Minerals And Tea Tree Pain Therapy
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 61995-0602?
What are the uses for Jason Cooling Minerals And Tea Tree Pain Therapy?
Which are Jason Cooling Minerals And Tea Tree Pain Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
Which are Jason Cooling Minerals And Tea Tree Pain Therapy 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:
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- MENTHOL (UNII: L7T10EIP3A)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- TEA TREE OIL (UNII: VIF565UC2G)
- EUROPEAN HAZELNUT OIL (UNII: 8RQ2839AVG)
- SOYBEAN OIL (UNII: 241ATL177A)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- SESAME OIL (UNII: QX10HYY4QV)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SAFFLOWER OIL (UNII: 65UEH262IS)
What is the NDC to RxNorm Crosswalk for Jason Cooling Minerals And Tea Tree Pain Therapy?
- RxCUI: 1297646 - methyl salicylate 13.5 % Topical Ointment
- RxCUI: 1297646 - methyl salicylate 0.135 MG/MG Topical Ointment
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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".