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: Safetec of America, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 96c41fc1-81f9-4757-abc6-867b5383ed5d
SPL ID: 10d3b150-077e-cb76-e063-6394a90ab356
Version: 6
Effective date: 2024-02-07
Source export date: 2026-10-30
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:33:26

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 · 19 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		Safetec of America, Inc.	openfda.manufacturer_name
ndc	package	61010-5600-2	openfda.package_ndc
ndc	package	61010-5600-1	openfda.package_ndc
ndc	package	61010-5600-4	openfda.package_ndc
ndc	package	61010-5600-3	openfda.package_ndc
ndc	product	61010-5600	openfda.product_ndc
ndc11	package	61010560004	derived:openfda.package_ndc
ndc11	package	61010560003	derived:openfda.package_ndc
ndc11	package	61010560002	derived:openfda.package_ndc
ndc11	package	61010560001	derived:openfda.package_ndc
rxcui		204602	openfda.rxcui
spl id		10d3b150-077e-cb76-e063-6394a90ab356	id
spl set id		96c41fc1-81f9-4757-abc6-867b5383ed5d	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 internally over large areas of the body if you are allergic to any of the ingredients longer than 1 week unless directed by a doctor Ask a doctor before use: in case of deep or puncture wounds, animal bites, or serious burns Stop use and ask a doctor if: the condition persists or gets worse a rash or other allergic reaction develops Keep this and all drugs out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a poison control center immediately.

Reported adverse events (FAERS/openFDA)#

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