Gold Bond Medicated Foot description, usages, side effects, indications, overdosage, supplying and lots more!

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Gold Bond Medicated Foot

Chattem, Inc.

Gold Bond Medicated Foot Spray




FULL PRESCRIBING INFORMATION

Drug Facts

Menthol (to deliver 1% concentration)

Anti-Itch

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

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

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

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)

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

Gold Bond Medicated Foot

Gold Bond Medicated Foot

Menthol SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41167-0172
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 1 g

Inactive Ingredients

Ingredient Name Strength
isobutane
propane
ALUMINUM STARCH OCTENYLSUCCINATE
talc
SODIUM BICARBONATE
benzethonium chloride
EUCALYPTUS OIL
ISOPROPYL MYRISTATE
PEPPERMINT OIL
PROPYLENE CARBONATE
ALCOHOL
SORBITAN MONOOLEATE
HECTORITE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41167-0172-2 100 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2001-12-01


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Be sure to consult your doctor before taking any medication!
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