PENIMIXCINA- bacitracin, neomycin sulfate, polymixin b sulfate, pramoxine hydrochloride ointment

PENIMIXCINA by

Drug Labeling and Warnings

PENIMIXCINA by is a Otc medication manufactured, distributed, or labeled by HEALTH LIFE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS (IN EACH GRAM)

BACITRACIN ZINC  500 UNITS

NEOMYCIN SULFATE  5 MG  (EQUIVALENT TO 3.5 MG NEOMYCIN)

POLYMYXIN B SULFATE  5000 UNITS

PRAMOXINE HYCHLORIDE  10 MG

PURPOSE

FIRST AID ANTIBIOTIC

PAIN RELIEVER

USES

• FIRST AID TO HELP PREVENT INFECTION IN
• MINOR CUTS
• SCRAPES
• BURNS

WARNINGS

For external use only.

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

• If swallowed get medical help or contact Poison Control Center 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

INACTIVE INGREDIENTS

WHITE PETROLATUM

OTHER INFORMATION

• STORE AT 15° - 30°C (59°F - 86°F)
• AVOID EXCESSIVE HEAT AND HUMIDITY

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PENIMIXCINA 
bacitracin, neomycin sulfate, polymixin b sulfate, pramoxine hydrochloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69517-615
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	500 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	5000 [iU]  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69517-615-05	1 in 1 BOX	09/05/2018
1	NDC: 69517-615-01	14 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 final	part333B	09/05/2018

Labeler - HEALTH LIFE (079656178)