Label: RALLI RAPID PAIN RELIEF- menthol liquid
- NDC Code(s): 63936-9509-1
- Packager: Troy Manufacturing, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 19, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Uses
-
Warnings
For external use only.Avoid contact with eyes.
Flammable:Keep away from fire or flame.
Contents under pressure: do not puncture or incinerate. Do not store at temperature above 120°F.
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
- 63936-9501
-
INGREDIENTS AND APPEARANCE
RALLI RAPID PAIN RELIEF
menthol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63936-9509 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 mL Inactive Ingredients Ingredient Name Strength INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) EUCALYPTUS OIL (UNII: 2R04ONI662) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) GLYCERIN (UNII: PDC6A3C0OX) PEG-8 DIMETHICONE (600 CST) (UNII: GIA7T764OD) PENTYLENE GLYCOL (UNII: 50C1307PZG) PEPPERMINT OIL (UNII: AV092KU4JH) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63936-9509-1 88 mL in 1 CAN; Type 0: Not a Combination Product 02/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 02/01/2024 Labeler - Troy Manufacturing, Inc. (160075248)