FDA.reportPublic FDA data

Dial Antibacterial Vitamin Bar

Manufacturer
Henkel Corporation
Effective date
2025-12-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:21:49

Label at a glance#

ProductDial Antibacterial Vitamin Bar
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

for washing to decrease the bacteria 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

Uses

INDICATIONS & USAGE SECTION

  • for washing to decrease the bacteria 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 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 Palm Kernelate* · Sodium Cocoate*] · Water · Glycerin · Stearic Acid* · Coconut Acid* · Palm Acid* · Palm Kernel Acid* · Fragrance · Sorbitol · Sodium Chloride · Tetrasodium Glutamate Diacetate · Tocopheryl Acetate · Panthenol · Alcohol · Retinyl Palmidate · Red 4 · Yellow 5

*Contains one or more of these ingredients

IngredientsIngredients

Questions?

OTC - QUESTIONS SECTION

1-800-253-DIAL (3425)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP Vitamins BarPDP Vitamins Bar

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1926450benzalkonium chloride 0.1 % Medicated Bar SoapPSN2
1926450benzalkonium chloride 0.001 MG/MG Medicated Bar SoapSCD2
1926450benzalkonium chloride 0.1 % Medicated Bar SoapSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54340-286-01Dial Antibacterial Vitamin Bar113 g in 1 CELLO PACKSOAP1132
54340-286-02Dial Antibacterial Vitamin Bar72 in 1 CASESOAP722

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54340-28654340-286-01, 54340-286-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
PANTHENOLWV9CM0O67ZIACT
RETINYL PALMITATE1D1K0N0VVCIACT
SORBITOL506T60A25RIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM PALM KERNELATE6H91L1NXTWIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT
SODIUM PALMATES0A6004K3ZIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
STEARIC ACID4ELV7Z65APIACT
FD&C RED NO. 4X3W0AM1JLXIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

Source Document#

Source XML

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 Vitamin BarDIAL ANTIBACTERIAL VITAMIN BAR SOAPHenkel Corporation292bf620-5cde-388d-e063-6394a90a307c2025-12-11WarningsExact identifier
ndc (package): 54340-286-02
ndc (package): 54340-286-01
ndc (product): 54340-286
ndc11 (package): 54340028601
ndc11 (package): 54340028602
spl id: 45af5199-620a-0642-e063-6294a90ad124
spl set id: 292bf620-5cde-388d-e063-6394a90a307c

Reported adverse events (FAERS/openFDA)#

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