FAMILY CARE TRIPLE ANTIBIOTIC ORIGINAL FORMULA 0.33OZ- triple antibiotic original formula ointment

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients (in each gram) Purpose
Bacitracin Zinc (400 units)........................................................First Aid Antibiotic
Neomycin Sulfate (3.5 mg).......................................................First Aid Antibiotic
Polymyxin B Sulfate (5,000 units).............................................First Aid Antibiotic

PURPOSE

Uses
first aid to help prevent infection in minor:
 cuts  scrapes  burns

WARNINGS

Warnings
For external use only.

DO NOT USE

Do not use
 in the eyes
 over large areas of the body
 if you are allergic to any of the ingredients

WHEN USING

Ask a doctor before use if you have
 deep or puncture wounds
 animal bites
 serious burns

STOP USE

Stop use and ask a doctor if
 condition persists or gets worse
 rash or other allergic reaction develops
 you need to use longer than 1 week

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

INDICATIONS & USAGE

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

STORAGE AND HANDLING

Other information
 store at 20° to 25°C (68° to 77°F)

INACTIVE INGREDIENT

Inactive ingredients
.alpha.-tocopherol acetate, methylparaben, petrolatum

DOSAGE & ADMINISTRATION

Questions or comments?
Call 1-888-645-8204 Monday-Friday 9AM-5PM (PST)
Distributed by: UNITED EXCHANGE CORP.
Cypress, CA 90630 USA | 1-888-645-8204
Made in China
688-ZDP-BX-R1
OM-TP-ZDP309-R1

KEEP OUT OF REACH OF CHILDREN

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FAMILY CARE TRIPLE ANTIBIOTIC ORIGINAL FORMULA 0.33OZ 
triple antibiotic original formula ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-577
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 [iU]  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	5000 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	3.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
METHYLPARABEN (UNII: A2I8C7HI9T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-577-33	1 in 1 BOX	04/10/2026
1		9.35 g in 1 TUBE; 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	04/10/2026

Labeler - United Exchange Corp (840130579)