Gold Bond Anti Itch description, usages, side effects, indications, overdosage, supplying and lots more!

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Gold Bond Anti Itch

Chattem, Inc.

Gold Bond Anti Itch




FULL PRESCRIBING INFORMATION

Drug Facts

Menthol 1%

Pramoxine hydrochloride 1%

Anti-itch, Pain relief

for temporary relief of pain and itching associated with:

  • minor skin irritations
  • minor cuts
  • minor burns
  • minor sunburns
  • rashes due to poison ivy, poison oak or poison sumac
  • scrapes
  • insect bites

For external use only

  • deep or puncture wounds
  • animals bites
  • serious burns
  • large areas of the body
  • do not get into eyes or nose
  • not for prolonged use
  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days
  • if redness, irritation, swelling or pain persists or increases

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

adults and children 2 years and older: apply to affected area up to 3 or 4 times daily

children under 2 years: consult a doctor

water, propylene glycol, petrolatum, stearyl alcohol, aloe barbadensis leaf juice, sodium acrylates copolymer, steareth-21, mineral oil, steareth-2, tocopheryl acetate, thymol, eucalyptol, methyl salicylate, PPG-1 trideceth-6,diazolidinyl urea, disodium EDTA, triethanolamine, iodopropynyl butylcarbamate (240-022)

ORIGINAL FORMULA GOLD BOND® MAXIMUM RELIEF
Net wt 1 oz (28 g)
ANTI-ITCH CREAM

Gold Bond Anti Itch

Gold Bond Anti Itch

Menthol and Pramoxine Hydrochloride CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41167-0501
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 0.01 g
pramoxine hydrochloride PRAMOXINE 0.01 g

Inactive Ingredients

Ingredient Name Strength
water
propylene glycol
petrolatum
stearyl alcohol
Aloe Vera Leaf
STEARETH-21
Mineral Oil
STEARETH-2
.ALPHA.-TOCOPHEROL ACETATE, D-
THYMOL
EUCALYPTOL
methyl salicylate
DIAZOLIDINYL UREA
EDETATE DISODIUM
IODOPROPYNYL BUTYLCARBAMATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 28 in 1 TUBE
2 35 in 1 TUBE
3 56 in 1 TUBE
4 NDC:41167-0501-2 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 1996-04-01


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Be sure to consult your doctor before taking any medication!
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