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, POLYMYXIN B SULFATE
Manufacturer: Acme United Corporation
Product type: HUMAN OTC DRUG
SPL set ID: f9a48f73-aa12-cf68-e053-6294a90a8e53
SPL ID: 27495546-006d-ad90-e063-6394a90a71ce
Version: 2
Effective date: 2024-11-19
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:15:41

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 · 25 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, POLYMYXIN B SULFATE	openfda.generic_name
manufacturer name		Acme United Corporation	openfda.manufacturer_name
ndc	package	0924-5604-00	openfda.package_ndc
ndc	package	0924-5604-04	openfda.package_ndc
ndc	package	0924-5604-05	openfda.package_ndc
ndc	package	0924-5604-01	openfda.package_ndc
ndc	package	0924-5604-03	openfda.package_ndc
ndc	package	0924-5604-06	openfda.package_ndc
ndc	package	0924-5604-02	openfda.package_ndc
ndc	product	0924-5604	openfda.product_ndc
ndc11	package	00924560403	derived:openfda.package_ndc
ndc11	package	00924560402	derived:openfda.package_ndc
ndc11	package	00924560406	derived:openfda.package_ndc
ndc11	package	00924560405	derived:openfda.package_ndc
ndc11	package	00924560400	derived:openfda.package_ndc
ndc11	package	00924560401	derived:openfda.package_ndc
ndc11	package	00924560404	derived:openfda.package_ndc
rxcui		204602	openfda.rxcui
spl id		27495546-006d-ad90-e063-6394a90a71ce	id
spl set id		f9a48f73-aa12-cf68-e053-6294a90a8e53	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 : in the eyes over large areas of the body on puncture wounds, animal bites, or serious burns longer than 1 week unless directed by a doctor if you are allergic to any of the ingredients Stop use and ask a doctor if: a rash or allergic reaction develops condition worsens or persists Keep out the reach of children.

Reported adverse events (FAERS/openFDA)#

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