Dial Professional Original Gold Antibacterial

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 Professional Original Gold Antibacterial
Generic name: DIAL PROFESSIONAL ORIGINAL GOLD ANTIBACTERIAL HAND SOAP
Manufacturer: Henkel Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 287965b6-5194-9d5c-e063-6394a90a4b68
SPL ID: 46150d5a-c8b1-6d8f-e063-6394a90a0d9d
Version: 2
Effective date: 2025-12-16
Source export date: 2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:26:38

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 Professional Original Gold Antibacterial	openfda.brand_name
generic name		DIAL PROFESSIONAL ORIGINAL GOLD ANTIBACTERIAL HAND SOAP	openfda.generic_name
manufacturer name		Henkel Corporation	openfda.manufacturer_name
ndc	package	54340-135-06	openfda.package_ndc
ndc	package	54340-135-11	openfda.package_ndc
ndc	package	54340-135-01	openfda.package_ndc
ndc	package	54340-135-03	openfda.package_ndc
ndc	package	54340-135-02	openfda.package_ndc
ndc	package	54340-135-09	openfda.package_ndc
ndc	package	54340-135-04	openfda.package_ndc
ndc	package	54340-135-08	openfda.package_ndc
ndc	package	54340-135-05	openfda.package_ndc
ndc	package	54340-135-12	openfda.package_ndc
ndc	package	54340-135-10	openfda.package_ndc
ndc	package	54340-135-07	openfda.package_ndc
ndc	product	54340-135	openfda.product_ndc
ndc11	package	54340013504	derived:openfda.package_ndc
ndc11	package	54340013505	derived:openfda.package_ndc
ndc11	package	54340013501	derived:openfda.package_ndc
ndc11	package	54340013503	derived:openfda.package_ndc
ndc11	package	54340013502	derived:openfda.package_ndc
ndc11	package	54340013509	derived:openfda.package_ndc
ndc11	package	54340013512	derived:openfda.package_ndc
ndc11	package	54340013511	derived:openfda.package_ndc
ndc11	package	54340013508	derived:openfda.package_ndc
ndc11	package	54340013506	derived:openfda.package_ndc
ndc11	package	54340013510	derived:openfda.package_ndc
ndc11	package	54340013507	derived:openfda.package_ndc
rxcui		1046593	openfda.rxcui
spl id		46150d5a-c8b1-6d8f-e063-6394a90a0d9d	id
spl set id		287965b6-5194-9d5c-e063-6394a90a4b68	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 Warnings For external use only When using this product•Avoid contact with eyes • Stop use and ask a doctor if•Irritation or redness develops OR Stop use and ask a doctor ifirritation or redness develops Keep out of reach of children. •If swallowed, get medical help or contact a Poison Control Center right away Warnings

Reported adverse events (FAERS/openFDA)#

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