Dial refresh and renew Antibacterial white

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 white
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Henkel Corporation
Product type: HUMAN OTC DRUG
SPL set ID: f7f5ed83-1b9b-230a-e053-6394a90ad2ae
SPL ID: 28f4db68-f795-4270-e063-6294a90ad4a0
Version: 2
Effective date: 2025-01-01
Source export date: 2026-10-12
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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:31:23

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 white	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Henkel Corporation	openfda.manufacturer_name
ndc	package	54340-260-03	openfda.package_ndc
ndc	package	54340-260-08	openfda.package_ndc
ndc	package	54340-260-04	openfda.package_ndc
ndc	package	54340-260-12	openfda.package_ndc
ndc	package	54340-260-01	openfda.package_ndc
ndc	product	54340-260	openfda.product_ndc
ndc11	package	54340026003	derived:openfda.package_ndc
ndc11	package	54340026012	derived:openfda.package_ndc
ndc11	package	54340026004	derived:openfda.package_ndc
ndc11	package	54340026008	derived:openfda.package_ndc
ndc11	package	54340026001	derived:openfda.package_ndc
rxcui		1926450	openfda.rxcui
spl id		28f4db68-f795-4270-e063-6294a90ad4a0	id
spl set id		f7f5ed83-1b9b-230a-e053-6394a90ad2ae	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.