Caring Mill Medicated Foot Powder -Talc Free

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]

MENTHOL- maximum strength medicated foot powder talc free powder 
FSA Store Inc.

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Caring Mill Medicated Foot Powder -Talc Free

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)

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	05/02/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/02/2023	05/02/2023

Labeler - FSA Store Inc. (049283340)

Revised: 12/2024

Document Id: 29ba8554-c5f1-4a05-e063-6394a90a520e

34390-5

Set id: fabc23eb-7750-1b5a-e053-6294a90aed03

Version: 2

Effective Time: 20241220