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: TRIFECTA PHARMACEUTICALS USA LLC
Product type: HUMAN OTC DRUG
SPL set ID: 23a35ba8-ebc6-4252-bb88-ec237425056c
SPL ID: 4f856706-7fa7-6db6-e063-6394a90a7f31
Version: 22
Effective date: 2026-04-15
Source export date: 2026-11-06
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:02:26

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 · 27 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		TRIFECTA PHARMACEUTICALS USA LLC	openfda.manufacturer_name
ndc	package	69396-002-25	openfda.package_ndc
ndc	package	69396-002-23	openfda.package_ndc
ndc	package	69396-002-09	openfda.package_ndc
ndc	package	69396-002-22	openfda.package_ndc
ndc	package	69396-002-05	openfda.package_ndc
ndc	package	69396-002-20	openfda.package_ndc
ndc	package	69396-002-33	openfda.package_ndc
ndc	package	69396-002-44	openfda.package_ndc
ndc	product	69396-002	openfda.product_ndc
ndc11	package	69396000220	derived:openfda.package_ndc
ndc11	package	69396000222	derived:openfda.package_ndc
ndc11	package	69396000205	derived:openfda.package_ndc
ndc11	package	69396000223	derived:openfda.package_ndc
ndc11	package	69396000225	derived:openfda.package_ndc
ndc11	package	69396000209	derived:openfda.package_ndc
ndc11	package	69396000233	derived:openfda.package_ndc
ndc11	package	69396000244	derived:openfda.package_ndc
rxcui		204602	openfda.rxcui
spl id		4f856706-7fa7-6db6-e063-6394a90a7f31	id
spl set id		23a35ba8-ebc6-4252-bb88-ec237425056c	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 ● if you are allergic to any of the ingredients. Ask a doctor before use if you have ● deep or puncture wounds ● animal bites ● serious burns. Stop use and ask a doctor if ● condition persists or gets worse ● you need to use longer than 1 week ● a rash or other allergic reaction develops

Reported adverse events (FAERS/openFDA)#

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