Kindest Kare Advanced Antimicrobial Foam Handwash

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: Kindest Kare Advanced Antimicrobial Foam Handwash
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: SC Johnson Professional USA, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 9ea1175e-45aa-45c5-87a1-55d64cc37a88
SPL ID: 1dbf475f-bc41-4beb-877a-4fe57d17ac10
Version: 9
Effective date: 2025-06-20
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 05:54:11

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 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Kindest Kare Advanced Antimicrobial Foam Handwash	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		SC Johnson Professional USA, Inc.	openfda.manufacturer_name
ndc	package	11084-807-67	openfda.package_ndc
ndc	package	11084-807-68	openfda.package_ndc
ndc	package	11084-807-13	openfda.package_ndc
ndc	package	11084-807-66	openfda.package_ndc
ndc	package	11084-807-27	openfda.package_ndc
ndc	package	11084-807-12	openfda.package_ndc
ndc	package	11084-807-41	openfda.package_ndc
ndc	product	11084-807	openfda.product_ndc
ndc11	package	11084080727	derived:openfda.package_ndc
ndc11	package	11084080768	derived:openfda.package_ndc
ndc11	package	11084080741	derived:openfda.package_ndc
ndc11	package	11084080767	derived:openfda.package_ndc
ndc11	package	11084080712	derived:openfda.package_ndc
ndc11	package	11084080766	derived:openfda.package_ndc
ndc11	package	11084080713	derived:openfda.package_ndc
spl id		1dbf475f-bc41-4beb-877a-4fe57d17ac10	id
spl set id		9ea1175e-45aa-45c5-87a1-55d64cc37a88	set_id
unii		F5UM2KM3W7	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 When using this product do not get it in the eyes; causes eye irritation upon direct contact. In case of eye exposure, rinse thoroughly with water. If eye irritation persists, contact a physician. Stop use and ask a doctor if irritation and redness develop and persist for more than 3 days. Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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