OLP Triple Antibiotic Plus

Manufacturer
Ohio Lab Pharma
Effective date
2018-11-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:57:23

Key Label Information#

Active Ingredients And Purpose

Active ingredients

Bacitracin zinc 400 units Neomycin 3.5 mg Polymyxin B sulfate 5,000 units Pramoxine hydrochloride 10 mg

Purpose

first aid antibiotic External Analgesic

Uses

USES

first aid to help prevent infection in minor • cuts • scrapes • burns

Warnings

Warnings

For external use only

Do not use

Do not use • if you are allergic to any of the ingredients • in the eyes • over large areas of the body • longer than 1 week unless directed by a doctor

Directions And Dosage

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 Label Information

Other information

Store at room temperature

Inactive ingredient

Petrolatum

Questions

www.ohiolabpharma.us

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Net Weight 0.33 oz (9.4g0 NDC#70648-121-01

Label Images#

triple antibiotic plus pain relief
triple antibiotic plus pain relief

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1999890bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5,000 UNT / pramoxine HCl 10 MG per GM Topical OintmentPSN3
1999890bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG / pramoxine hydrochloride 0.01 MG/MG Topical OintmentSCD3
1999890bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5,000 UNT / pramoxine hydrochloride 10 MG per GM Topical OintmentSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BACITRACIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
NEOMYCIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
POLYMYXIN B Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
99e684e6-f435-feb8-d2bb-3a546f1cb768Product name220161117
25340b3b-3e4c-4ff8-abf6-3e62ec46bd0cProduct name120160603
2d352c73-a357-4193-a4de-dfdf9a2ac8e4Product name120150819
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
b6082387-f592-1148-0844-bd068fd213fbProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70648-121-012020-01-31C16284748780-19d75b9cf-f8d8-f424-e053-dadaa90a57ce5fb447d6-dbbf-6745-e053-2a91aa0ae0bf

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70648-121-01OLP Triple Antibiotic Plus9.4 g in 1 TUBEOINTMENT9.43
70648-121-01OLP Triple Antibiotic Plus1 in 1 CARTONOINTMENT13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70648-121OLP TRIPLE ANTIBIOTIC PLUS (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, LIDOCAINE) OINTMENT [OHIO LAB PHARMA]3Legacy NDC, 2 package rows20181127_5fb447d6-dbbf-6745-e053-2a91aa0ae0bf.zip

Products#

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70648-12170648-121-01

Ingredients#

Complete SPL Sections#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Bacitracin zinc 400 units Neomycin 3.5 mg Polymyxin B sulfate 5,000 units Pramoxine hydrochloride 10 mg

USES

INDICATIONS & USAGE SECTION

first aid to help prevent infection in minor • cuts • scrapes • burns

Purpose

OTC - PURPOSE SECTION

first aid antibiotic External Analgesic

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use • if you are allergic to any of the ingredients • in the eyes • over large areas of the body • longer than 1 week unless directed by a doctor

OTC - ASK DOCTOR SECTION

OTC - ASK DOCTOR SECTION

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

OTC - STOP USE SECTION

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

STORAGE AND HANDLING SECTION

Store at room temperature

Inactive ingredient

INACTIVE INGREDIENT SECTION

Petrolatum

Questions

OTC - QUESTIONS SECTION

www.ohiolabpharma.us

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Net Weight 0.33 oz (9.4g0 NDC#70648-121-01

Source Document#

Source XML