Dial Antibacterial Bar

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 Antibacterial Bar
Generic name: DIAL WHITE ANTIBACTERIAL BAR SOAP
Manufacturer: Henkel Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 5691b718-bb66-1529-e054-00144ff88e88
SPL ID: 43806e83-a91f-da54-e063-6294a90a3e7b
Version: 14
Effective date: 2025-11-13
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 05:54:31

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 · 33 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Dial Antibacterial Bar	openfda.brand_name
generic name		DIAL WHITE ANTIBACTERIAL BAR SOAP	openfda.generic_name
manufacturer name		Henkel Corporation	openfda.manufacturer_name
ndc	package	54340-278-19	openfda.package_ndc
ndc	package	54340-278-13	openfda.package_ndc
ndc	package	54340-278-12	openfda.package_ndc
ndc	package	54340-278-14	openfda.package_ndc
ndc	package	54340-278-16	openfda.package_ndc
ndc	package	54340-278-10	openfda.package_ndc
ndc	package	54340-278-06	openfda.package_ndc
ndc	package	54340-278-11	openfda.package_ndc
ndc	package	54340-278-09	openfda.package_ndc
ndc	package	54340-278-08	openfda.package_ndc
ndc	package	54340-278-04	openfda.package_ndc
ndc	package	54340-278-15	openfda.package_ndc
ndc	product	54340-278	openfda.product_ndc
ndc11	package	54340027804	derived:openfda.package_ndc
ndc11	package	54340027819	derived:openfda.package_ndc
ndc11	package	54340027812	derived:openfda.package_ndc
ndc11	package	54340027810	derived:openfda.package_ndc
ndc11	package	54340027811	derived:openfda.package_ndc
ndc11	package	54340027816	derived:openfda.package_ndc
ndc11	package	54340027813	derived:openfda.package_ndc
ndc11	package	54340027809	derived:openfda.package_ndc
ndc11	package	54340027808	derived:openfda.package_ndc
ndc11	package	54340027806	derived:openfda.package_ndc
ndc11	package	54340027815	derived:openfda.package_ndc
ndc11	package	54340027814	derived:openfda.package_ndc
rxcui		1926450	openfda.rxcui
spl id		43806e83-a91f-da54-e063-6294a90a3e7b	id
spl set id		5691b718-bb66-1529-e054-00144ff88e88	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 eyes. In case of eye contact, flush with water. Stop using and ask doctor if irritation or redness develops Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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