Sheffield 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: Sheffield Triple Antibiotic
Generic name: BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE
Manufacturer: Sheffield Pharmaceuticals LLC
Product type: HUMAN OTC DRUG
SPL set ID: 1aa95046-c1f7-4fc7-acac-839065d998f6
SPL ID: e78cd65b-8aeb-4fc5-8551-2deceb5d01e2
Version: 6
Effective date: 2025-02-17
Source export date: 2026-10-27
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:50:52

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		Sheffield Triple Antibiotic	openfda.brand_name
generic name		BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE	openfda.generic_name
manufacturer name		Sheffield Pharmaceuticals LLC	openfda.manufacturer_name
ndc	package	11527-162-55	openfda.package_ndc
ndc	package	11527-162-51	openfda.package_ndc
ndc	package	11527-162-30	openfda.package_ndc
ndc	package	11527-162-47	openfda.package_ndc
ndc	package	11527-162-27	openfda.package_ndc
ndc	product	11527-162	openfda.product_ndc
ndc11	package	11527016255	derived:openfda.package_ndc
ndc11	package	11527016230	derived:openfda.package_ndc
ndc11	package	11527016247	derived:openfda.package_ndc
ndc11	package	11527016227	derived:openfda.package_ndc
ndc11	package	11527016251	derived:openfda.package_ndc
rxcui		204602	openfda.rxcui
spl id		e78cd65b-8aeb-4fc5-8551-2deceb5d01e2	id
spl set id		1aa95046-c1f7-4fc7-acac-839065d998f6	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 Allergy alert: do not use if you are allergic to any of the ingredients Do not use in or near the eyes on large areas of the body Consult a doctor before use if you have deep or puncture wounds animal bites serious burns When using this product do not use longer than 1 week Stop use and consult a doctor if condition persists or gets worse symptoms last for more than 7 days or clear up and come back within a few days a rash or other allergic reaction develops Keep out of the 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.