NEOMYCIN- neomycin ointment ointment

Neomycin by

Drug Labeling and Warnings

Neomycin by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Label

1164-25

INGREDIENTS AND APPEARANCE

NEOMYCIN 
neomycin ointment ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-218
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WHITE PETROLATUM (UNII: B6E5W8RQJ4)

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-218-01	1000 in 1 CASE	01/30/2024
1	NDC: 67777-218-02	10 in 1 BOX
1		0.9 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 67777-218-03	1800 in 1 CASE	01/30/2024
2	NDC: 67777-218-04	25 in 1 BOX
2		0.9 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	01/30/2024

Labeler - Dynarex Corporation (008124539)