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 FSA Store Inc.. 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 irritations

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.

If swallowed, 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 1-866-964-0939

Principal Display Panel

Caring Mill

maximum strength

medicated

foot powder

external analgesic/menthol 1 %

talc- free

triple action formula

• absorbs moisture
• relieve itching
• helps control foot odor

NET WT 10 OZ (283 g)

INGREDIENTS AND APPEARANCE

MENTHOL 
maximum strength medicated foot powder talc free powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81522-075
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
ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
BENZETHONIUM CHLORIDE (UNII: PH41D05744)
EUCALYPTUS OIL (UNII: 2R04ONI662)
PEPPERMINT OIL (UNII: AV092KU4JH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81522-075-01	283 g in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package	05/02/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	05/02/2023

Labeler - FSA Store Inc. (049283340)