Neosporin Plus Pain Relief Clubtray

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 Plus Pain Relief Clubtray
Generic name: BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE
Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
SPL set ID: f4545718-8643-a340-e053-2995a90a0079
SPL ID: 4d4ac333-666f-cb35-e063-6294a90a35ef
Version: 3
Effective date: 2026-03-18
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 19:52:34

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		Neosporin Plus Pain Relief Clubtray	openfda.brand_name
generic name		BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Kenvue Brands LLC	openfda.manufacturer_name
ndc	package	69968-0801-9	openfda.package_ndc
ndc	package	69968-0057-2	openfda.package_ndc
ndc	package	69968-0057-1	openfda.package_ndc
ndc	product	69968-0801	openfda.product_ndc
ndc11	package	69968080109	derived:openfda.package_ndc
ndc11	package	69968005702	derived:openfda.package_ndc
ndc11	package	69968005701	derived:openfda.package_ndc
rxcui		1359350	openfda.rxcui
spl id		4d4ac333-666f-cb35-e063-6294a90a35ef	id
spl set id		f4545718-8643-a340-e053-2995a90a0079	set_id

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 symptoms persist for more than 1 week, or clear up and occur again within a few days rash or other allergic reaction develops Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Centre right away.

Reported adverse events (FAERS/openFDA)#

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