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Family Care Antibiotic by United Exchange Corp.

Medically reviewed on December 29, 2017

Dosage form: ointment
Ingredients: NEOMYCIN SULFATE 3.5mg in 1g
Labeler: United Exchange Corp.
NDC Code: 65923-517

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.

Family Care Antibiotic Ointment 513

Active ingredient (in each gram) Purpose

Neomycin sulfate 3.5 mg...................................................................First Aid-Antibiotic


For external use only


first aid to help prevent infection in:

  • minor cuts
  • scrapes
  • burns

Do not use

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

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

Stop use and ask a doctor if

  • you need to use longer than 1 week
  • rash or other allergic reaction develops
  • the condition persists or gets worse

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.


  • 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

Other information

  • ‚Äčstore between 20° to 25°C (68° to 77°F)
  • Lot No. & Exp. Date: see box or see crimp of tube

Inactive ingredients

cetanol, ethanol, liquid paraffin, methylparaben, petrolatum, propylparaben, purified lanolin, squalane, tocopherol acetate

Distributed by:

United Exchange Corp.

17211 Valley View Ave.

Cerritos, CA 90703 USA

1 800 814 8028

Made in Korea

neomycin sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-517
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:65923-517-281 TUBE in 1 BOX
128 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B12/29/2017
Labeler - United Exchange Corp. (840130579)

United Exchange Corp.

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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.