MENTHOL- maximum strength medicated foot powder powder

Menthol by

Drug Labeling and Warnings

Menthol by is a Otc medication manufactured, distributed, or labeled by VALU MERCHANDISERS, CO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Active ingredient

Menthol 1.0%

Purpose

External analgesic

​Use

for the temporary relief of pain and itching associated with minor skin irritation on the foot

​Warnings

​For external use only.

When using this product

• avoid contact with eyes

Stop and consult a doctor if

• conditions worsens
• symptoms persists for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

​Directions

• adults and children 2 years of age and older, apply to affected area not more than 3 to 4 times daily
• children under 2 years of age, consult a doctor
• wash and dry feet thoroughly
• sprinkle powder liberally on feet, between toes and on bottoms of feet

​Inactive ingredients

benzethonium chloride, eucalytus oil, gum acacia, peppermint oil, sodium bicarbonate, talc

​Questions?

Call 1-866-964-0939

Principal Display Panel

Best Choice

Medicated

Foot Powder

Menthol 1.0% External Analgesic

Triple Relief Formula

• Absorbs Moisture
• Relieves Itching
• Controls Foot Odor

NET WT 10 OZ (283 g)

INGREDIENTS AND APPEARANCE

MENTHOL 
maximum strength medicated foot powder powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63941-552
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2.8 g  in 283 g

Inactive Ingredients
Ingredient Name	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744)
EUCALYPTUS OIL (UNII: 2R04ONI662)
ACACIA (UNII: 5C5403N26O)
PEPPERMINT OIL (UNII: AV092KU4JH)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
TALC (UNII: 7SEV7J4R1U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63941-552-10	283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/12/2017	09/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	12/12/2017	09/26/2020

Labeler - VALU MERCHANDISERS, CO (868703513)