MENTHOL- maximum strength medicated foot powder talc free powder

Menthol by

Drug Labeling and Warnings

Menthol by is a Otc medication manufactured, distributed, or labeled by Topco Associates LLC. 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

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

benzathonium Chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, zea mays (corn) starch

Questions?

Call - 1-888-423-0139

Principal Display Panel

TopCare health

MAXIMUM STRENGTH

Medicated Foot Powder

MENTHOL 1%

EXTERNAL ANALGESIC

TALC-FREE

Triple-Action Formula

• Absorbs Moisture
• Relieves Itching
• Helps Control Foot Odor

NET WT 10 OZ (283g)

INGREDIENTS AND APPEARANCE

MENTHOL 
maximum strength medicated foot powder talc free powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 36800-252
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
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
BENZETHONIUM CHLORIDE (UNII: PH41D05744)
PEPPERMINT OIL (UNII: AV092KU4JH)
EUCALYPTUS OIL (UNII: 2R04ONI662)
ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 36800-252-10	283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/10/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/10/2019

Labeler - Topco Associates LLC (006935977)