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Triple Antibiotic Plus Pain Relief

Kroger Company

TRIPLE ANTIBIOTIC OINTMENTPLUS PAIN RELIEF●Bacitracin Zinc ●Neomycin Sulfate ●Polymyxin B Sulfate ●Pramoxine Hydrochloride




FULL PRESCRIBING INFORMATION

Drug Facts

Bacitracin zinc 500 units
Neomycin 3.5 mg
Polymyxin B sulfate 10,000 units
Pramoxine hydrochloride 10 mg

First aid antibiotic/Pain reliever

helps prevent infection in and temporarily relieves pain due to

  • minor cuts
  • scrapes
  • burns

For external use only

  •  do not use if allergic to any of the ingredients
  • in or near  the eyes
  • on large areas of the body
  • deep or puncture wounds
  • animal bites
  • serious burns
  • do not use longer than 1 week
  • condition lasts 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 occurs

Keep out of reach of children. 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 (equal to surface area of tip of finger) on area 1 to 3 times daily
  • may be covered with a sterile bandage

Children under 2 years: ask a doctor

white petrolatum

Kroger®
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

Helps prevent infection in minor cuts, scrapes, and burns plus topical pain reliever.

NET WT 1 OZ (28 g)

Triple Antibiotic Plus Pain Relief

Triple Antibiotic Plus Pain Relief

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

Product Information

Product Type Human otc drug label Item Code (Source) NDC:30142-823
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:30142-823-56 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partB part333B 2008-07-24


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