Triple Antibiotic plus Pain Relief Maximum Strength

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Triple Antibiotic plus Pain Relief Maximum Strength
Generic name: BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE
Manufacturer: Chain Drug Consortium, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 55ef2205-aaf1-4aa4-917f-2b4cfa43b77e
SPL ID: c6bc1e43-7d2c-460d-9465-b17efe3c50ad
Version: 9
Effective date: 2025-07-01
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:37:32

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		Triple Antibiotic plus Pain Relief Maximum Strength	openfda.brand_name
generic name		BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Chain Drug Consortium, LLC	openfda.manufacturer_name
ndc	package	68016-715-01	openfda.package_ndc
ndc	product	68016-715	openfda.product_ndc
ndc11	package	68016071501	derived:openfda.package_ndc
rxcui		1359350	openfda.rxcui
spl id		c6bc1e43-7d2c-460d-9465-b17efe3c50ad	id
spl set id		55ef2205-aaf1-4aa4-917f-2b4cfa43b77e	set_id
unii		89Y4M234ES	openfda.unii
unii		057Y626693	openfda.unii
unii		88AYB867L5	openfda.unii
unii		19371312D4	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use if you are allergic to any of the ingredients in the eyes over large areas of the body Ask a doctor before use if you have deep or puncture wounds animal bites serious burns Stop use and ask a doctor if you need to use longer than one week condition persists or gets worse rash or other allergic reaction develops symptoms persist for more than one week, or clear up and occur again within a few days Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.