RALLI RAPID PAIN RELIEF- menthol liquid

Ralli Rapid Pain Relief by

Drug Labeling and Warnings

Ralli Rapid Pain Relief by is a Otc medication manufactured, distributed, or labeled by Troy Manufacturing, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Menthol 10.0%

Purpose

Topical Analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with:  simple backache  arthritis  strains  bruises  sprains

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

Stop use and ask a doctor if

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days  redness is present  excessive irritation of the skin develops

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 2 years of age and older:  apply directly onto affected area without the need to rub, massage or bandage  repeat if necessary, but do not apply more than 3 to 4 times daily.

Children under 2 years of age: do not use, consult a doctor.

Other Information

store at room temperature

Inactive Ingredients

boswellia serrata extract, dimethylsulfone (MSM), eucalyptus oil, glucosamine sulfate, glycerin, PEG-8 dimethicone, pentylene glycol, peppermint oil, SD alcohol 39C, water (USP).

63936-9501

INGREDIENTS AND APPEARANCE

RALLI RAPID PAIN RELIEF 
menthol liquid

Product 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)