Neosporin Plus Pain Relief First Aid Antibiotic/Pain Relieving

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 First Aid Antibiotic/Pain Relieving
Generic name: NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE
Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
SPL set ID: 23222e54-d793-4d79-980e-550e32a95742
SPL ID: 223ce228-cc0e-5108-e063-6294a90a4aea
Version: 7
Effective date: 2024-11-13
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:38

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		M017	openfda.application_number
brand name		Neosporin Plus Pain Relief First Aid Antibiotic/Pain Relieving	openfda.brand_name
generic name		NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Kenvue Brands LLC	openfda.manufacturer_name
ndc	package	69968-0055-1	openfda.package_ndc
ndc	package	69968-0055-2	openfda.package_ndc
ndc	product	69968-0055	openfda.product_ndc
ndc11	package	69968005501	derived:openfda.package_ndc
ndc11	package	69968005502	derived:openfda.package_ndc
rxcui		1359360	openfda.rxcui
spl id		223ce228-cc0e-5108-e063-6294a90a4aea	id
spl set id		23222e54-d793-4d79-980e-550e32a95742	set_id
unii		057Y626693	openfda.unii
unii		88AYB867L5	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 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.