Label: CAMPHOTREX- camphor, menthol gel
- NDC Code(s): 59088-283-07
- Packager: PureTek Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 11, 2023
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- Active Ingredients (% by weight)
- Purpose
- Uses
- Warnings
- Directions
- Other information
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Inactive ingredients
Acrylates Copolymer, Alcohol Denat., Boswellia Serrata Extract, Chondroitin Sulfate, Eucalyptus Globulus Leaf Oil, Glucosamine Sulfate, Glycerin, Ilex Paraguariensis (Yerba Mate), Magnesium Chloride, Mentha Piperita (Peppermint) Oil, MSM (Methylsulfonylmethane), Propylene Glycol, Triethanolamine, Water.
- Camphotrex®
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INGREDIENTS AND APPEARANCE
CAMPHOTREX
camphor, menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-283 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 4 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10 g in 100 g Inactive Ingredients Ingredient Name Strength METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C) ALCOHOL (UNII: 3K9958V90M) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z) EUCALYPTUS OIL (UNII: 2R04ONI662) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) GLYCERIN (UNII: PDC6A3C0OX) ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) PEPPERMINT OIL (UNII: AV092KU4JH) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-283-07 85 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 04/12/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/12/2016 Labeler - PureTek Corporation (785961046)