Neosporin Original

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: Neosporin Original
Generic name: BACITRACIN ZINC, NEOMYCIN SULFATE, AND POLYMYXIN B SULFATE
Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
SPL set ID: f07d3bca-4312-46ed-b0c4-f886c01bd095
SPL ID: 21fa7843-fca7-30ab-e063-6294a90ad79e
Version: 3
Effective date: 2024-11-14
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:24:10

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		Neosporin Original	openfda.brand_name
generic name		BACITRACIN ZINC, NEOMYCIN SULFATE, AND POLYMYXIN B SULFATE	openfda.generic_name
manufacturer name		Kenvue Brands LLC	openfda.manufacturer_name
ndc	package	69968-0634-9	openfda.package_ndc
ndc	package	69968-0634-1	openfda.package_ndc
ndc	product	69968-0634	openfda.product_ndc
ndc11	package	69968063409	derived:openfda.package_ndc
ndc11	package	69968063401	derived:openfda.package_ndc
rxcui		204602	openfda.rxcui
spl id		21fa7843-fca7-30ab-e063-6294a90ad79e	id
spl set id		f07d3bca-4312-46ed-b0c4-f886c01bd095	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 if you are allergic to any of the ingredients in the eyes over large areas of the body 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.