Label: STOPAIN CLINICAL- menthol gel
- NDC Code(s): 63936-9758-1
- Packager: Troy Manufacturing, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 25, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Uses
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Warnings
Avoid contact with eyes. For external use only.
Flammable: Keep away from fire or flame.
When using this product
- use only as directed
- do not bandage tightly or use a heating pad
- do not apply to wounds or damaged skin
- Directions
- Other Information
- Inactive Ingredients
- Package Labeling:
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INGREDIENTS AND APPEARANCE
STOPAIN CLINICAL
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63936-9758 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 100 mg in 1 g Inactive Ingredients Ingredient Name Strength ACRYLIC ACID (UNII: J94PBK7X8S) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) EUCALYPTUS OIL (UNII: 2R04ONI662) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH) PEG-8 DIMETHICONE (UNII: GIA7T764OD) PENTYLENE GLYCOL (UNII: 50C1307PZG) PEPPERMINT OIL (UNII: AV092KU4JH) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63936-9758-1 3 g in 1 PACKET; Type 0: Not a Combination Product 11/30/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/30/2022 Labeler - Troy Manufacturing, Inc. (160075248)