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NDC 41415-0051-75 Publix 500 [iU]/g Details

Publix 500 [iU]/g

Publix is a TOPICAL OINTMENT in the HUMAN OTC DRUG category. It is labeled and distributed by Publix Super Markets Inc. The primary component is BACITRACIN ZINC.

MedlinePlus Drug Summary

Bacitracin is used to help prevent minor skin injuries such as cuts, scrapes, and burns from becoming infected. Bacitracin is in a class of medications called antibiotics. Bacitracin works by stopping the growth of bacteria.

Related Packages: 41415-0051-75
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Bacitracin Topical

Product Information

NDC	41415-0051
Product ID	41415-051_24cb11f4-9b28-4fe5-bf6b-54b70eaaf1e1
Associated GPIs	46100010101820
GCN Sequence Number	003026
GCN Sequence Number Description	magnesium hydroxide ORAL SUSP 400 MG/5ML ORAL
HIC3	D6S
HIC3 Description	LAXATIVES AND CATHARTICS
GCN	07950
HICL Sequence Number	001329
HICL Sequence Number Description	MAGNESIUM HYDROXIDE
Brand/Generic	Generic
Proprietary Name	Publix
Proprietary Name Suffix	Bacitracin Zinc
Non-Proprietary Name	Bacitracin Zinc
Product Type	HUMAN OTC DRUG
Dosage Form	OINTMENT
Route	TOPICAL
Active Ingredient Strength	500
Active Ingredient Units	[iU]/g
Substance Name	BACITRACIN ZINC
Labeler Name	Publix Super Markets Inc
Pharmaceutical Class	Decreased Cell Wall Synthesis & Repair [PE]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333B
Listing Certified Through	2023-12-31

Package

Package Images

NDC 41415-0051-75 (41415005175)

Pricing Information	N/A
NDC Package Code	41415-051-75
Billing NDC	41415005175
Package	1 TUBE in 1 CARTON (41415-051-75) / 28.4 g in 1 TUBE
Marketing Start Date	2006-05-11
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 5d76ce12-042d-4669-9fe7-6ff074f31232 Details

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (each gram contains)

Bacitracin Zinc 500 units

Purpose

First aid antibiotic

Uses

first aid to help prevent infection in

minor cuts
scrapes
burns

Warnings

For external use only

Do not use

in the eyes
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

on deep or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if

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 right away.

Directions

clean the affected area and dry thoroughly
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

To open: unscrew cap, pull tab to remove foil seal
store at room temperature
see carton or tube crimp for lot number and expiration date

Inactive ingredients

mineral oil, white petrolatum

Questions?

Call 1-866-923-4914

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY PUBLIX

SUPER MARKETS, INC.

3300 PUBLIX CORPORATE

PARKWAY

LAKELAND, FL 33811

PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton

Publix

bacitracinzinc

OINTMENT USP

FIRST AID ANTIBIOTIC OINTMENT

• helps prevent infection in minor cuts, scrapes, and burns.

NET WT 1 OZ (28.4 g)

PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton

INGREDIENTS AND APPEARANCE

PUBLIX BACITRACIN ZINC

bacitracin zinc ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:41415-051
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Bacitracin Zinc (UNII: 89Y4M234ES) (Bacitracin - UNII:58H6RWO52I)	Bacitracin	500 [iU] in 1 g

Ingredient Name	Strength
Inactive Ingredients
mineral oil (UNII: T5L8T28FGP)
petrolatum (UNII: 4T6H12BN9U)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:41415-051-75	1 in 1 CARTON	05/11/2006
1		28.4 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part333B	05/11/2006

Labeler - Publix Super Markets Inc (006922009)

Registrant - Taro Pharmaceuticals U.S.A., Inc. (145186370)

Name	Address	ID/FEI	Business Operations
Establishment
Taro Pharmaceuticals Inc.		206263295	MANUFACTURE(41415-051)

Revised: 12/2021

Document Id: 24cb11f4-9b28-4fe5-bf6b-54b70eaaf1e1

Set id: 5d76ce12-042d-4669-9fe7-6ff074f31232

Version: 2

Effective Time: 20211215

Search by Drug Name or NDC

NDC 41415-0051-75 Publix 500 [iU]/g Details

Publix 500 [iU]/g

MedlinePlus Drug Summary

Product Information

Package

Package Images

NDC 41415-0051-75 (41415005175)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 5d76ce12-042d-4669-9fe7-6ff074f31232 Details

SPL UNCLASSIFIED SECTION

Active ingredient (each gram contains)

Purpose

Uses

Warnings

Do not use

Ask a doctor before use

Stop use and ask a doctor if

Directions

Other information

Inactive ingredients

Questions?

SPL UNCLASSIFIED SECTION

PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton

INGREDIENTS AND APPEARANCE

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