First Aid Only 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: First Aid Only Triple Antibiotic
Generic name: BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE
Manufacturer: Acme United Corporation
Product type: HUMAN OTC DRUG
SPL set ID: f4eba34c-ce31-3004-e053-2995a90a245b
SPL ID: 2749912f-9bf8-7cf9-e063-6394a90a5a94
Version: 3
Effective date: 2024-11-19
Source export date: 2026-10-12
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:25:46

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		First Aid Only Triple Antibiotic	openfda.brand_name
generic name		BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	openfda.generic_name
manufacturer name		Acme United Corporation	openfda.manufacturer_name
ndc	package	0924-5618-03	openfda.package_ndc
ndc	package	0924-5618-04	openfda.package_ndc
ndc	package	0924-5618-00	openfda.package_ndc
ndc	package	0924-5618-02	openfda.package_ndc
ndc	product	0924-5618	openfda.product_ndc
ndc11	package	00924561804	derived:openfda.package_ndc
ndc11	package	00924561802	derived:openfda.package_ndc
ndc11	package	00924561803	derived:openfda.package_ndc
ndc11	package	00924561800	derived:openfda.package_ndc
rxcui		204602	openfda.rxcui
spl id		2749912f-9bf8-7cf9-e063-6394a90a5a94	id
spl set id		f4eba34c-ce31-3004-e053-2995a90a245b	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 longer than 1 week unless directed by a doctor on deep lacerations or puncture wounds, animal bites, or serious burns Stop use and ask a doctor if condition persists or gets worse a rash or allergic reaction occurs the condition persists for more than 7 days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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