Triple Antibiotic

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
Generic name: BACITRACIN ZINC, NEOMYCIN SULFATE, AND POLYMYXIN B SULFATE
Manufacturer: Acme United Corporation
Product type: HUMAN OTC DRUG
SPL set ID: e55cbf7e-c955-7f1a-e053-2a95a90a3f28
SPL ID: 27497a82-401e-7cb5-e063-6394a90a87c1
Version: 2
Effective date: 2024-11-19
Source export date: 2026-11-06
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/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:08:55

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		Triple Antibiotic	openfda.brand_name
generic name		BACITRACIN ZINC, NEOMYCIN SULFATE, AND POLYMYXIN B SULFATE	openfda.generic_name
manufacturer name		Acme United Corporation	openfda.manufacturer_name
ndc	package	0924-5610-00	openfda.package_ndc
ndc	package	0924-5610-02	openfda.package_ndc
ndc	package	0924-5610-01	openfda.package_ndc
ndc	product	0924-5610	openfda.product_ndc
ndc11	package	00924561001	derived:openfda.package_ndc
ndc11	package	00924561002	derived:openfda.package_ndc
ndc11	package	00924561000	derived:openfda.package_ndc
rxcui		204602	openfda.rxcui
spl id		27497a82-401e-7cb5-e063-6394a90a87c1	id
spl set id		e55cbf7e-c955-7f1a-e053-2a95a90a3f28	set_id
unii		89Y4M234ES	openfda.unii
unii		057Y626693	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 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 •on deep lacerations or puncture wounds, animal bites, or serious burns STOP USE AND ASK A DOCTOR IF •condition persists or gets worse •a rash or allergic reaction occurs •condition persists for more than 7 days Keep out the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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