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, POLYMYXIN B
Manufacturer: Padagis Israel Pharmaceuticals Ltd
Product type: HUMAN OTC DRUG
SPL set ID: 28fff253-ddd4-4669-aa90-b4caf48c905f
SPL ID: 007b5d54-72af-4d4e-a893-c6a79396b9b3
Version: 7
Effective date: 2024-09-22
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:29

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, POLYMYXIN B	openfda.generic_name
manufacturer name		Padagis Israel Pharmaceuticals Ltd	openfda.manufacturer_name
ndc	package	45802-143-00	openfda.package_ndc
ndc	package	45802-143-01	openfda.package_ndc
ndc	package	45802-143-70	openfda.package_ndc
ndc	package	45802-143-03	openfda.package_ndc
ndc	product	45802-143	openfda.product_ndc
ndc11	package	45802014300	derived:openfda.package_ndc
ndc11	package	45802014301	derived:openfda.package_ndc
ndc11	package	45802014370	derived:openfda.package_ndc
ndc11	package	45802014303	derived:openfda.package_ndc
rxcui		204602	openfda.rxcui
spl id		007b5d54-72af-4d4e-a893-c6a79396b9b3	id
spl set id		28fff253-ddd4-4669-aa90-b4caf48c905f	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 • 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 1 week • condition persists or gets worse • rash or other allergic reaction develops Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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