GOLD BOND MEDICATED FOOT- menthol spray 
Chattem, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Gold Bond Medicated Foot Spray

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%)

PRINCIPAL DISPLAY PANEL
Maximum Strength 
GOLD BOND FOOT SPRAY
NET WT. 3.5 OZ. (100 g) (Menthol 1%)

GOLD BOND MEDICATED FOOT 
menthol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0172
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-0172-2100 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/01/200104/30/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34812/01/200104/30/2012
Labeler - Chattem, Inc. (003336013)

Revised: 12/2020
 
Chattem, Inc.