GOLD BOND MEDICATED MAXIMUM STRENGTH FOOT- menthol powder

Gold Bond Medicated Maximum Strength Foot by

Drug Labeling and Warnings

Gold Bond Medicated Maximum Strength Foot by is a Otc medication manufactured, distributed, or labeled by Gold Bond Co LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Gold Bond Medicated

Maximum Strength Foot Powder

Drug Facts

Active ingredient

Menthol 1%

Purpose

Anti-itch

Uses

temporarily relieves the pain and itch associated with:

■ minor skin irritations on the foot  

Warnings

For external use only

When using this product

■ avoid contact with eyes  

Stop use and ask a doctor if

■ condition worsens

■ symptoms persist for more than 7 days or clear up and occur again within a few days

■ redness, irritation, swelling or pain persists or increases

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

■ adults and children 2 years and older: apply freely up to 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 bottoms of feet. Sprinkle inside shoes for maximum freshness.

Inactive ingredients

zea mays (corn) starch, sodium bicarbonate, acacia senegal gum, silica, tricalcium phosphate, eucalyptus globulus leaf oil, mentha piperita (peppermint) oil, benzethonium chloride

PRINCIPAL DISPLAY PANEL

GOLD BOND
MEDICATED
MAXIMUM STRENGTH
FOOT POWDER
ANTI-ITCH MENTHOL 1%
TRIPLE ACTION FORMULA
Net Wt 10 oz (283 g)

INGREDIENTS AND APPEARANCE

GOLD BOND MEDICATED MAXIMUM STRENGTH FOOT 
menthol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84714-0171
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
STARCH, CORN (UNII: O8232NY3SJ)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
ACACIA (UNII: 5C5403N26O)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
EUCALYPTUS OIL (UNII: 2R04ONI662)
PEPPERMINT OIL (UNII: AV092KU4JH)
BENZETHONIUM CHLORIDE (UNII: PH41D05744)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84714-0171-2	283 g in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2021
2	NDC: 84714-0171-6	113 g in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/01/2021

Labeler - Gold Bond Co LLC (119184861)