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

Triple Antibiotic Plus

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  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert



FULL PRESCRIBING INFORMATION

(in each gram)

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

Allergy alert:

  • 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

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

  • Store at 59º - 86ºF (15º - 30ºC).

White petrolatum

1-800-432-8534 (select option #2) between 9 am and 4 pm EST, Monday-Friday.

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*Compare to the active ingredients in Neosporin® Plus Ointment

MAXIMUM STRENGTH

TRIPLE ANTIBIOTIC OINTMENT + PAIN RELIEF

FIRST AID ANTIBIOTIC/PAIN RELIEVING OINTMENT

(Bacitracin Zinc – Neomycin Sulfate - Polymyxin B Sulfate - Pramoxine HCl)

Net Wt 1 oz (28 g)

08230809E1 VC109660


                  
               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:55301-823
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:55301-823-56 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partB part333B 2005-03-01


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