WALGREENS MEDICATED FOOT POWDER- menthol powder

Walgreens Medicated Foot Powder by

Drug Labeling and Warnings

Walgreens Medicated Foot Powder by is a Otc medication manufactured, distributed, or labeled by Davion, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Menthol 1.0%

Purpose

External Analgesic

Uses

For the temporary relief of pain and itch associate with minor skin irritations on the foot

Warning

• For external use only

When using this product

• avoid contact with eyes

Stop use and ask a doctor if

• condition 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 and older - apply freely upto 3 or 4 times daily
• children under 2 years - ask a doctor
  
  Thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottom of feet and in shoes

Inactive ingredients

Talc, Sodium Bicarbonate, Acacia, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil

Principal Display Panel

NDC: 42669-100-10

WALGREENS FOOT POWDER

Compare to Gold Bond Medicated Foot Powder active ingredient

Foot Powder

MENTHOL 1.0%/ EXTERNAL ANALGESIC

MAXIMUM STRENGTH

MEDICATED

Absorbs Moisture
Helps control foot odor

NET WT 10 OZ (283 g)

INGREDIENTS AND APPEARANCE

WALGREENS MEDICATED FOOT POWDER 
menthol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42669-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42669-100-10	283 g in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/01/2018

Labeler - Davion, Inc (174542928)

Registrant - Davion, Inc (174542928)

Establishment
Name	Address	ID/FEI	Business Operations
Davion, Inc		174542928	manufacture(42669-100)