Bacitracin Zinc

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: Bacitracin Zinc
Generic name: FIRST AID ANTIBIOTIC
Manufacturer: Aldermed Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 7f4bff4f-588d-4e45-8aa3-f95b4d746f25
SPL ID: 53c0eec1-bde8-470f-e063-6294a90a29f0
Version: 5
Effective date: 2026-06-08
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 05:55:42

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		Bacitracin Zinc	openfda.brand_name
generic name		FIRST AID ANTIBIOTIC	openfda.generic_name
manufacturer name		Aldermed Inc.	openfda.manufacturer_name
ndc	package	87236-001-44	openfda.package_ndc
ndc	package	87236-001-14	openfda.package_ndc
ndc	package	87236-001-15	openfda.package_ndc
ndc	package	87236-001-09	openfda.package_ndc
ndc	package	87236-001-01	openfda.package_ndc
ndc	product	87236-001	openfda.product_ndc
ndc11	package	87236000114	derived:openfda.package_ndc
ndc11	package	87236000144	derived:openfda.package_ndc
ndc11	package	87236000109	derived:openfda.package_ndc
ndc11	package	87236000101	derived:openfda.package_ndc
ndc11	package	87236000115	derived:openfda.package_ndc
rxcui		1366116	openfda.rxcui
spl id		53c0eec1-bde8-470f-e063-6294a90a29f0	id
spl set id		7f4bff4f-588d-4e45-8aa3-f95b4d746f25	set_id
unii		89Y4M234ES	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 or apply 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 if you have deep or puncture wounds, animal bites, or serious burns Stop use and ask a doctor if the condition persists or gets worse if a 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.

Reported adverse events (FAERS/openFDA)#

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