Triple Antibiotic Plus description, usages, side effects, indications, overdosage, supplying and lots more!

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Triple Antibiotic Plus

The Kroger Co.




FULL PRESCRIBING INFORMATION

(in each gram)

Bacitracin zinc, USP 500 units

Neomycin Sulfate, USP 3.5 mg

Polymyxin B sulfate, USP 10,000 units

Pramoxine hydrochloride, USP 10 mg

First aid antibiotic/Pain reliever

First aid to help prevent infection and for temporary relief of pain or discomfort due to

  • minor cuts
  • scrapes
  • burns

For external use only

Allergy alert:

  • do not use if allergic to any of the ingredients
  • in the eyes
  • over large areas of the body
  • deep or puncture wounds
  • animal bites
  • serious burns[/S][/S][/S]
  • do not use longer than 1 week unless directed by a doctor
  • condition persists or gets worse
  • symptoms last for more than 7 days or clear up and come back within a few days
  • a rash or other allergic reaction develops

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

Adults and children 2 years and older:

  • clean affected area
  • apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on area 1 to 3 times daily
  • may be covered with a sterile bandage

Children under 2 years: ask a doctor

  • Store at 59º -86ºF (15º -30ºC).
  • Before using any medication, read all label directions. Keep carton, it contains important information.

White petrolatum

1-800-632-6900

Kroger ®

QUALITY GUARANTEED

Compare to the active ingredients of NEOSPORIN® PLUS.

*See Back Panel.

maximum strength

TRIPLE ANTIBIOTIC OINTMENT

PLUS PAIN RELIEF

• Bacitracin Zinc • Neomycin Sulfate • Polymyxin B Sulfate • Pramoxine Hydrochloride

• First aid antibiotic plus topical pain reliever

NET WT 1 OZ (28 g)

08230611xx VC108014

  • Triple Antibiotic Plus

CARTON LABEL

Triple Antibiotic Plus

bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59450-823
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BACITRACIN ZINC BACITRACIN 500 [USP'U]
Neomycin Sulfate NEOMYCIN 3.5 mg
Polymyxin B Sulfate POLYMYXIN B 10000 [USP'U]
pramoxine hydrochloride PRAMOXINE 10 mg

Inactive Ingredients

Ingredient Name Strength
petrolatum

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 28 in 1 TUBE
2 NDC:59450-823-56 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partB part333B 2008-07-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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