Rexall 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: Rexall Antibiotic
Generic name: BACITRACIN
Manufacturer: Dolgencorp, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 7ad42602-6e42-47c8-91a8-e4785fa8d24b
SPL ID: 0b3913da-2bc7-4d3f-88cd-8b2005863fde
Version: 6
Effective date: 2024-09-23
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:19:37

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		Rexall Antibiotic	openfda.brand_name
generic name		BACITRACIN	openfda.generic_name
manufacturer name		Dolgencorp, LLC	openfda.manufacturer_name
ndc	package	55910-536-64	openfda.package_ndc
ndc	product	55910-536	openfda.product_ndc
ndc11	package	55910053664	derived:openfda.package_ndc
rxcui		1648110	openfda.rxcui
spl id		0b3913da-2bc7-4d3f-88cd-8b2005863fde	id
spl set id		7ad42602-6e42-47c8-91a8-e4785fa8d24b	set_id
unii		58H6RWO52I	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 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.

Reported adverse events (FAERS/openFDA)#

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