Drugplain

PENIMIXCINA 500 [iU]/g

BACITRACIN, NEOMYCIN SULFATE, POLYMIXIN B SULFATE, PRAMOXINE HYDROCHLORIDE · OINTMENT · OPMX LLC

No Recall History
Plain English

PENIMIXCINA is a ointment containing bacitracin, neomycin sulfate, polymixin b sulfate, pramoxine hydrochloride at 500 [iU]/g, taken topical. Manufactured by OPMX LLC.

Key Facts

Brand Name
PENIMIXCINA
Generic Name
BACITRACIN, NEOMYCIN SULFATE, POLYMIXIN B SULFATE, PRAMOXINE HYDROCHLORIDE
NDC Code (Product)
69729-615
Manufacturer
OPMX LLC
Strength
500 [iU]/g
Dosage Form
OINTMENT
Route
TOPICAL
Marketing Status
Application #
M004
Marketing Start
09/05/2018

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

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

Dosage & Administration

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

Warnings

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

Frequently Asked Questions

What is PENIMIXCINA used for?

PENIMIXCINA contains BACITRACIN, NEOMYCIN SULFATE, POLYMIXIN B SULFATE, PRAMOXINE HYDROCHLORIDE. It is a ointment taken topical. Consult your doctor for specific uses.

Is PENIMIXCINA a controlled substance?

PENIMIXCINA is not classified as a controlled substance by the DEA.

What is the generic name for PENIMIXCINA?

The generic name for PENIMIXCINA is BACITRACIN, NEOMYCIN SULFATE, POLYMIXIN B SULFATE, PRAMOXINE HYDROCHLORIDE. There are no other listed brand versions of BACITRACIN, NEOMYCIN SULFATE, POLYMIXIN B SULFATE, PRAMOXINE HYDROCHLORIDE.

What is the NDC code for PENIMIXCINA 500 [iU]/g?

The NDC (National Drug Code) for PENIMIXCINA 500 [iU]/g is 69729-615, listed by OPMX LLC.

Product NDC

69729-615

Package NDC

69729-615-05

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)