MAXIMUM STRENGTH MEDICATED FOOT POWDER- medicated foot powder powder

Maximum Strength Medicated Foot Powder by

Drug Labeling and Warnings

Maximum Strength Medicated Foot Powder by is a Otc medication manufactured, distributed, or labeled by Target Corporation. 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 1-800-910-6874

Principal Display Panel

Maximum strength

medicated

foot powder

menthol 1%
external analgesic

triple relief formula helps absorb moisture
helps relieve itching and control foot odor

NET WT 10 OZ (283g)

INGREDIENTS AND APPEARANCE

MAXIMUM STRENGTH MEDICATED FOOT POWDER 
medicated foot powder powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-510
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.1 g  in 1 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: 11673-510-10	283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/30/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/30/2013

Labeler - Target Corporation (006961700)