Dial refresh and renew Antibacterial Bar Spring Water

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: Dial refresh and renew Antibacterial Bar Spring Water
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Henkel Corporation
Product type: HUMAN OTC DRUG
SPL set ID: f8390069-3899-908f-e053-6294a90ad2fb
SPL ID: 2825ba00-f02e-b15b-e063-6394a90afe81
Version: 2
Effective date: 2024-11-20
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:51:47

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Dial refresh and renew Antibacterial Bar Spring Water	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Henkel Corporation	openfda.manufacturer_name
ndc	package	54340-300-08	openfda.package_ndc
ndc	package	54340-300-12	openfda.package_ndc
ndc	package	54340-300-01	openfda.package_ndc
ndc	package	54340-300-04	openfda.package_ndc
ndc	package	54340-300-03	openfda.package_ndc
ndc	product	54340-300	openfda.product_ndc
ndc11	package	54340030012	derived:openfda.package_ndc
ndc11	package	54340030008	derived:openfda.package_ndc
ndc11	package	54340030001	derived:openfda.package_ndc
ndc11	package	54340030004	derived:openfda.package_ndc
ndc11	package	54340030003	derived:openfda.package_ndc
rxcui		1926450	openfda.rxcui
spl id		2825ba00-f02e-b15b-e063-6394a90afe81	id
spl set id		f8390069-3899-908f-e053-6294a90ad2fb	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 • avoid contact with the eyes. In case of eye contact, flush with water. Stop use and ask a doctor if • irritation and redness 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.