FDA.reportPublic FDA data

Dial Antibacterial Bar Soap - Gold

Manufacturer
Henkel Corporation
Effective date
2026-11-02
Label type
HUMAN OTC DRUG LABEL
Version
13
Source
daily-update
Hydrated at
2026-11-05 03:02:13

Label at a glance#

ProductDial Antibacterial Bar
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

• for washing to decrease the bacterial on the skin

Dosage and administration

• wet bar with water • lather vigorously and wash skin • rinse and dry thoroughly

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Dial Gold AntibacterialDial Gold Antibacterial

Uses

INDICATIONS & USAGE SECTION

• for washing to decrease the bacterial on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

• avoid contact with eyes. In case of eye contact, flush with water.

Stop using and ask doctor if

OTC - STOP USE SECTION

• irritation or redness develops

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• wet bar with water
• lather vigorously and wash skin
• rinse and dry thoroughly

Inactive ingredients:

INACTIVE INGREDIENT SECTION


Soap [Sodium Palmate* · Sodium Cocoate* · Sodium Palm Kernelate*] · Water · Glycerin · Coconut Acid* · Palm Acid* · Palm Kernel Acid* · Stearic Acid* · Fragrance · Sorbitol · Sodium Chloride · Tetrasodium Glutamate Diacetate · Titanium Dioxide · Yellow 5 · Alcohol · Yellow 8 · Red 4
*Contains one or more of these ingredients

Dial Gold inactive ingredientsDial Gold inactive ingredients

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dial Gold DFBDial Gold DFB

Dial Gold PDPDial Gold PDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130017000024028GTIN-13: 0017000024028
EAN-13: 0017000024028
GTIN-12: 017000024028
UPC-A: 017000024028
GTIN storage (14 digits): 00017000024028		Dial bar Gold DFB Art.jpg
QR code linkQR Codesk-qr.com/DIALQRDial bar Gold FOP Art.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54340-27254340-272-22, 54340-272-39, 54340-272-02, 54340-272-38, 54340-272-20, 54340-272-36, 54340-272-05, 54340-272-41, 54340-272-28, 54340-272-21, 54340-272-37, 54340-272-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
EXT. D&C YELLOW NO. 708F8S9O3I5IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM PALM KERNELATE6H91L1NXTWIACT
SORBITOL506T60A25RIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
STEARIC ACID4ELV7Z65APIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
ALCOHOL3K9958V90MIACT
CI 14700X3W0AM1JLXIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
122025-11-13full-release2026-06-01 01:16:11

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dial Antibacterial BarDIAL GOLD ANTIBACTERIAL BAR SOAPHenkel Corporation9e52beca-e8f2-3fa8-e053-2995a90aedd72025-11-13WarningsExact identifier
ndc (package): 54340-272-05
ndc (package): 54340-272-41
ndc (package): 54340-272-01
ndc (package): 54340-272-28
ndc (package): 54340-272-22
ndc (package): 54340-272-38
ndc (package): 54340-272-39
ndc (package): 54340-272-20
ndc (package): 54340-272-36
ndc (package): 54340-272-02
ndc (package): 54340-272-37
ndc (package): 54340-272-21
ndc (product): 54340-272
ndc11 (package): 54340027205
ndc11 (package): 54340027201
ndc11 (package): 54340027241
ndc11 (package): 54340027237
ndc11 (package): 54340027221
ndc11 (package): 54340027222
ndc11 (package): 54340027220
ndc11 (package): 54340027238
ndc11 (package): 54340027236
ndc11 (package): 54340027239
ndc11 (package): 54340027228
ndc11 (package): 54340027202
spl set id: 9e52beca-e8f2-3fa8-e053-2995a90aedd7

Reported adverse events (FAERS/openFDA)#

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