NEOMYCIN- neomycin ointment ointment 
Dynarex Corporation

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1164UB-10
1164-25

Active Ingredient (in each gram)

Neomycin Sulfate 5mg (equivalent to 3.5 mg Neomycin)

Purpose

First Aid Antibiotic

Use(s)

First aid to help prevent infection in minor cuts, scrapes, and burns

Warnings

For External Use Only

Do not use

• In the eyes or over large areas of the body

• If you are allergic to any of the ingredients

• Longer than 1 week unless directed by a doctor

Ask a doctor before use if

You have deep or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if

• The condition persists or gets worse

• A rash or other allergic reaction develops

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• 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

• Store at room temperature between 15º-30ºC (59º-86ºF)

• Tamper evident. Do not use if seal is torn, cut, or opened.

Inactive Ingredient(s)

White Petrolatum

Questions?

1-888-396-2739 Monday - Friday, 9AM - 5PM EST.

Label

1164UB-10_BX_MASTER1164UB-10

Label

1164-25_BX_MASTER1164-25

NEOMYCIN 
neomycin ointment ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-218
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
Product Characteristics
Color    Score    
ShapeFREEFORMSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-218-011000 in 1 CASE01/30/2024
1NDC:67777-218-0210 in 1 BOX
10.9 g in 1 PACKET; Type 0: Not a Combination Product
2NDC:67777-218-031800 in 1 CASE01/30/2024
2NDC:67777-218-0425 in 1 BOX
20.9 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00401/30/2024
Labeler - Dynarex Corporation (008124539)

Revised: 1/2024
Document Id: 0f9e087b-6e87-a3c7-e063-6394a90ac8d4
Set id: 0f9e087b-6e86-a3c7-e063-6394a90ac8d4
Version: 1
Effective Time: 20240123
 
Dynarex Corporation