NDC 77108-103 Medistik Cooling Roll-on
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77108 - Medistik Inc
- 77108-103 - Medistik Cooling Roll-on
Product Packages
NDC Code 77108-103-11
Package Description: 89 mL in 1 BOTTLE
Product Details
What is NDC 77108-103?
What are the uses for Medistik Cooling Roll-on?
Which are Medistik Cooling Roll-on UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR OIL (UNII: 75IZZ8Y727)
- CAMPHOR OIL (UNII: 75IZZ8Y727) (Active Moiety)
Which are Medistik Cooling Roll-on 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- GLYCERIN (UNII: PDC6A3C0OX)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- CHONDROITIN SULFATE (CHICKEN) (UNII: 7VZ9466BAB)
- FOLIC ACID (UNII: 935E97BOY8)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- VITAMIN D (UNII: 9VU1KI44GP)
What is the NDC to RxNorm Crosswalk for Medistik Cooling Roll-on?
- RxCUI: 2370887 - camphor 4 % / menthol 10 % Topical Solution
- RxCUI: 2370887 - camphor 40 MG/ML / menthol 100 MG/ML Topical Solution
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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".