Dial refresh and renew Antibacterial

Manufacturer
Henkel Corporation
Effective date
2024-12-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:48:08

Label at a glance#

ProductDial refresh and renew Antibacterial Mountain Fresh
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

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

Use

INDICATIONS & USAGE SECTION

• for washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product • avoid contact with eyes. In case of eye contact, flush with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if • irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of chlidren. 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 palm kernelate* • sodium cocoate*] • water • glycerin • stearic acid* • coconut acid* • palm acid* • palm kernel acid* • fragrance • titanium dioxide • sortibol • sodium chloride • tetrasodium glutamate diacetate • alcohol • yellow 5 • green 3

*contains one or more of these ingredients

Questions?

OTC - QUESTIONS SECTION

1-800-258-DIAL (3425)

SPL UNCLASSIFIED SECTION

Dial ® refresh & renew™

DEODORANT BAR SOAP

ANTIBACTERIAL

mountain fresh ®

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

®, TM, © 2023 Distributed by

Henkel Corporation, Rocky Hill, CT 06067

Made in Colombia

3-4 OZ SOAP BARS (113g), TOTAL NET WT 12 OZ (339g)

labellabel

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 Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54340-017-03Dial refresh and renew AntibacterialMountain Fresh113 g in 1 PACKETSOAP1132
54340-017-03Dial refresh and renew AntibacterialMountain Fresh3 in 1 PACKAGESOAP32
54340-017-08Dial refresh and renew AntibacterialMountain Fresh113 g in 1 PACKETSOAP1132
54340-017-08Dial refresh and renew AntibacterialMountain Fresh8 in 1 PACKAGESOAP82

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54340-017DIAL REFRESH AND RENEW ANTIBACTERIAL MOUNTAIN FRESH (BENZALKONIUM CHLORIDE) SOAP [HENKEL CORPORATION]2Current NDC, 4 package rows20241222_f9a347aa-808c-2095-e053-6394a90a58b1.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54340-01754340-017-03, 54340-017-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

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 refresh and renew Antibacterial Mountain FreshBENZALKONIUM CHLORIDEHenkel Corporationf9a347aa-808c-2095-e053-6394a90a58b12024-12-10WarningsExact identifier
ndc (package): 54340-017-03
ndc (package): 54340-017-08
ndc (product): 54340-017
ndc11 (package): 54340001708
ndc11 (package): 54340001703
spl id: 28f4a243-ce2d-80e8-e063-6394a90a1ce0
spl set id: f9a347aa-808c-2095-e053-6394a90a58b1

Reported adverse events (FAERS/openFDA)#

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