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

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Triple Antibiotic Plus Pain Relief

Navarro Discount Pharmacies,LLC

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients (in each gram)





Purpose

First aid antibiotic

First aid antibiotic

First aid antibiotic

External analgesic

Triple Antibiotic Plus Pain Relief Uses


  • cuts
  • scrapes
  • burns

Warnings

For external use only

Do not use

  • if you are allergic to any of the ingredients
  • in the eyes
  • over large areas of the body

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

  • you need to use longer than 1 week
  • condition persists or gets worse
  • condition persists for more than 1 week, or clear up and occur again within a few days
  • a rash or other allergic reaction develops

Keep out of reach of children.

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

Directions

  • adults and children 2 years of age and older:
    • clean the affected area
    • apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily
    • may be covered with a sterile bandage
  • children under 2 years of age: consult a physician

Triple Antibiotic Plus Pain Relief Other information

Inactive ingredient

white petrolatum

PRINCIPAL DISPLAY PANEL

Triple Antibiotic Ointment Plus Pain ReliefTriple Antibiotic Plus Pain Relief

Triple Antibiotic Plus Pain Relief

Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59970-040
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 28.3 in 1 TUBE
2 NDC:59970-040-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partB part333B 2012-08-01


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