GOLD BOND MEDICATED FOOT- menthol spray

Gold Bond Medicated Foot by

Drug Labeling and Warnings

Gold Bond Medicated Foot by is a Otc medication manufactured, distributed, or labeled by Chattem, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Menthol (to deliver 1% concentration)

Purpose

Anti-Itch

Uses

temporarily relieves the pain and itch associated with minor skin irritations on the foot

• Provides maximum strength itch relief
  
• Absorbs excess moisture
  
• Helps control foot odor and odor-causing bacteria
  
• Cools and soothes irritated skin

Warnings

For external use only

• Avoid spraying in eyes or on mucous membranes.

Flammable mixture

• Contents under pressure
  
• Do not puncture or incinerate
  
• Do not use near fire or flame
  
• Do not expose to heat or temperatures above 49ºC (120ºF)
  
• Use only as directed

Stop use and ask a doctor if

• condition worsens
  
• symptoms do not get better within 7 days

Keep out of reach of children.

Directions

• adults and children 2 years and older
  
• apply freely up to 3 to 4 times daily
  
• Thoroughly wash and dry feet
  
• Shake well
  
• Hold 6 inches from feet and spray generously over feet, between toes, on bottoms of feet, and in socks and shoes
  
• Use daily
  
• children under 2 years ask a doctor

Other information

Store at room temperature 15º-30ºC (59º-86ºF)

Inactive ingredients

isobutane, propane, alcohol SD-40B (12% w/w), aluminum starch octenylsuccinate, talc, sodium bicarbonate, benzethonium chloride, eucalyptus globules leaf oil, isopropyl myristate, menthe piperita (peppermint) oil, propylene carbonate, sorbitan oleate, stearylkonium hectorite. (227-078)

PRINCIPAL DISPLAY PANEL

MAXIMUM STRENGTH GOLD BOND FOOT SPRAY
MEDICATED HEALING SINCE 1908TM
TRIPLE ACTION RELIEF
NET WT. 3.5 OZ. (100 g) (Menthol 1%)

INGREDIENTS AND APPEARANCE

GOLD BOND MEDICATED FOOT 
menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41167-0172
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
ISOBUTANE (UNII: BXR49TP611)
PROPANE (UNII: T75W9911L6)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
TALC (UNII: 7SEV7J4R1U)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
BENZETHONIUM CHLORIDE (UNII: PH41D05744)
EUCALYPTUS OIL (UNII: 2R04ONI662)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PEPPERMINT OIL (UNII: AV092KU4JH)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
ALCOHOL (UNII: 3K9958V90M)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
HECTORITE (UNII: 08X4KI73EZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41167-0172-2	100 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/01/2001

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part348	12/01/2001

Labeler - Chattem, Inc. (003336013)