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 GOLD ANTIBACTERIAL BAR SOAP
Manufacturer: Henkel Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 9e52beca-e8f2-3fa8-e053-2995a90aedd7
SPL ID: 437d7bd6-37b8-1a35-e063-6394a90a64c2
Version: 12
Effective date: 2025-11-13
Source export date: 2026-10-30
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:41:09

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 GOLD ANTIBACTERIAL BAR SOAP	openfda.generic_name
manufacturer name		Henkel Corporation	openfda.manufacturer_name
ndc	package	54340-272-05	openfda.package_ndc
ndc	package	54340-272-41	openfda.package_ndc
ndc	package	54340-272-01	openfda.package_ndc
ndc	package	54340-272-28	openfda.package_ndc
ndc	package	54340-272-22	openfda.package_ndc
ndc	package	54340-272-38	openfda.package_ndc
ndc	package	54340-272-39	openfda.package_ndc
ndc	package	54340-272-20	openfda.package_ndc
ndc	package	54340-272-36	openfda.package_ndc
ndc	package	54340-272-02	openfda.package_ndc
ndc	package	54340-272-37	openfda.package_ndc
ndc	package	54340-272-21	openfda.package_ndc
ndc	product	54340-272	openfda.product_ndc
ndc11	package	54340027205	derived:openfda.package_ndc
ndc11	package	54340027201	derived:openfda.package_ndc
ndc11	package	54340027241	derived:openfda.package_ndc
ndc11	package	54340027237	derived:openfda.package_ndc
ndc11	package	54340027221	derived:openfda.package_ndc
ndc11	package	54340027222	derived:openfda.package_ndc
ndc11	package	54340027220	derived:openfda.package_ndc
ndc11	package	54340027238	derived:openfda.package_ndc
ndc11	package	54340027236	derived:openfda.package_ndc
ndc11	package	54340027239	derived:openfda.package_ndc
ndc11	package	54340027228	derived:openfda.package_ndc
ndc11	package	54340027202	derived:openfda.package_ndc
rxcui		1926450	openfda.rxcui
spl id		437d7bd6-37b8-1a35-e063-6394a90a64c2	id
spl set id		9e52beca-e8f2-3fa8-e053-2995a90aedd7	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 a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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