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Lincoln by Lincoln Pharmaceuticals Ltd.

Medically reviewed on April 9, 2018

Dosage form: ointment
Ingredients: BACITRACIN ZINC 500[USP'U] in 1g
Labeler: Lincoln Pharmaceuticals Ltd.
NDC Code: 69636-3035

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.

Drug Facts

Active Ingredient (in each gram)

Bacitracin Zinc (equal to 500 bacitracin units)

Drug Facts

First Aid Antibiotic

Drug Facts

Uses

  • first aid to help prevent infection in minor
  • cuts scrapes
  • burns

Drug Facts

For External use only

Do not use

  • in the eyes
  • if you are allergenic to any of the ingredients
  • over large area of the body longer than 1 week unless directed by a doctor

Drug Facts
  • deep or puncture wounds
  • animal bites
  • serious burns

Drug Facts
  • the condition persists or get worse
  • a rash or other allergic reaction develops

Drug Facts

Keep out of reach of children

  • if swallowed, get medical help or Contact a Poison Control Center right away

Drug Facts
  • clean the affected area
  • apply a small amount of this product (an amount equals 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

Drug Facts

Other information:

  • store at controlled temperature 15°-30° C
  • Avoid excessive heat and humidity

Drug Facts

Inactive ingredients

hard paraffin, liquid paraffin, white soft paraffin, lanolin

Principal Display Panel

LINCOLN 
bacitracin zinc ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69636-3035
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
MINERAL OIL 
LANOLIN 
PETROLATUM 
PARAFFIN 
Packaging
#Item CodePackage Description
1NDC:69636-3035-20.9 g in 1 PACKET
2NDC:69636-3035-314 g in 1 TUBE
3NDC:69636-3035-428 g in 1 TUBE
4NDC:69636-3035-5113 g in 1 TUBE
5NDC:69636-3035-6425 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B05/30/2013
Labeler - Lincoln Pharmaceuticals Ltd. (915839373)
Establishment
NameAddressID/FEIOperations
Lincoln Pharmaceuticals Ltd915839373manufacture(69636-3035)

 
Lincoln Pharmaceuticals Ltd.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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