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Bacitracin Zinc by Blossom Pharmaceuticals

Dosage form: ointment
Ingredients: BACITRACIN ZINC 500[USP'U] in 1g
Labeler: Blossom Pharmaceuticals
NDC Code: 61767-220

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Bacitracin Zinc Ointment

Active ingredient                         Purpose
Bacitracin Zinc 500 Units                Antibiotic

Warnings:

For external use only

Dosage & Administration

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

Indications & Usage
  • if you are allergic to any of the ingredients
  • in the eyes
  • over large areas of the body
  • longer than 1 week unless directed by a doctor

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center right away

Purpose:

First aid to help prevent infection in:

  • Minor cuts
  • scrapes
  • burns

Ask a doctor before use:
  • in case of deep or puncture wounds
  • animal bites
  • serious burns

Other information
  • store at controlled room temperature 15°-30° C (59°-86° F)

Stop Use and ask a doctor if
  • the condition persists or gets worse, or if a rash or other allergic reaction develops.

Inactive ingredients

Hard Paraffin, Liquid Paraffin, White Soft Paraffin

Principal Display Panel

Blossom Pharmaceuticals Bacitracin Zinc Ointment:

bacitracin zinc.jpg


BACITRACIN ZINC 
bacitracin zinc ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61767-220
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (BACITRACIN) BACITRACIN500 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM 
LIGHT MINERAL OIL 
MINERAL OIL 
Packaging
#Item CodePackage Description
1NDC:61767-220-0228.35 g in 1 TUBE
2NDC:61767-220-0314.17 g in 1 TUBE
3NDC:61767-220-04113.4 g in 1 TUBE
4NDC:61767-220-07425.3 g in 1 JAR
5NDC:61767-220-050.5 g in 1 PACKET
6NDC:61767-220-010.9 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B05/14/2014
Labeler - Blossom Pharmaceuticals (677381470)
Establishment
NameAddressID/FEIOperations
Blossom Pharmaceuticals677381470manufacture(61767-220)

 
Blossom Pharmaceuticals

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Medically reviewed on May 14, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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