Xpect 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: Xpect Triple Antibiotic
Generic name: BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE
Manufacturer: Cintas Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 39355db3-24d7-485f-9ce0-f0e466e96593
SPL ID: a3c837b5-b59a-4853-979e-dca5ec565cf9
Version: 3
Effective date: 2025-09-26
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:34:09

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		Xpect Triple Antibiotic	openfda.brand_name
generic name		BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	openfda.generic_name
manufacturer name		Cintas Corporation	openfda.manufacturer_name
ndc	package	42961-236-03	openfda.package_ndc
ndc	package	42961-236-04	openfda.package_ndc
ndc	package	42961-236-02	openfda.package_ndc
ndc	package	42961-236-01	openfda.package_ndc
ndc	product	42961-236	openfda.product_ndc
ndc11	package	42961023603	derived:openfda.package_ndc
ndc11	package	42961023604	derived:openfda.package_ndc
ndc11	package	42961023601	derived:openfda.package_ndc
ndc11	package	42961023602	derived:openfda.package_ndc
rxcui		204602	openfda.rxcui
spl id		a3c837b5-b59a-4853-979e-dca5ec565cf9	id
spl set id		39355db3-24d7-485f-9ce0-f0e466e96593	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 longer than 1 week unless directed by a doctor if you are allergic to any of the ingredients Ask a doctor before use in case of deep 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 condition clears up and occurs again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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