Dove

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-05-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:12:43

Label at a glance#

ProductDove
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For washing to decrease bacteria on the skin

Dosage and administration

Wet bar with water, lather vigorously and use all over body. Rinse clean.

Label contents#

Full prescribing information#

DOVE CARE & PROTECT ANTIBACTERIAL BEAUTY BAR - Benzalkonium Chloride soap

DESCRIPTION SECTION

Dove Care & Protect Antibacterial Beauty Bar

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium Chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

• For external use only
• When using this product
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with wate r
• Stop use and ask doctor
if irritation or redness develop.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children except under adult supervision.

If swallowed, get medical help or contact a poison control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet bar with water, lather vigorously and use all over body. Rinse clean.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sodium Lauroyl Isethionate, Stearic Acid, Sodium Oleate, Sodium Stearate, Water (Aqua), Sodium Isethionate, Lauric Acid, Sodium C14-16 Olefin Sulfonate, Sodium Laurate, Fragrance (Parfum), Dipropylene Glycol, Sodium Chloride, Tetrasodium Etidronate, Tetrasodium EDTA, Kaolin*, Titanium Dioxide*, Blue 1 (CI 42090), Yellow 5 (CI 19140). *Contains one or more of these ingredients

Questions or Comments?

OTC - QUESTIONS SECTION

1-800-761-3683

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dove Antibacterial Beauty BarDove Antibacterial Beauty Bar

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2057666benzalkonium chloride 0.13 % Medicated Bar SoapPSN3
2057666benzalkonium chloride 0.0013 MG/MG Medicated Bar SoapSCD3
2057666benzalkonium chloride 0.13 % Medicated Bar SoapSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1845-1Dove270 g in 1 CARTONSOAP2703
64942-1845-2Dove425 g in 1 CARTONSOAP4253
64942-1845-3Dove636 g in 1 CARTONSOAP6363
64942-1845-4Dove212 g in 1 CARTONSOAP2123
64942-1845-5Dove600 g in 1 CARTONSOAP6003
64942-1845-6Dove425 g in 1 CARTONSOAP4253

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1845DOVE (CARE AND PROTECT ANTIBACTERIAL BEAUTY BAR) SOAP [CONOPCO INC. D/B/A/ UNILEVER]3Legacy NDC, 6 package rows20240518_b9e248d7-0df3-649d-e053-2a95a90a0d0f.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-184564942-1845-1, 64942-1845-2, 64942-1845-3, 64942-1845-4, 64942-1845-5, 64942-1845-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
18a7d8ff-39bf-14fd-e063-6294a90a6182b9e248d7-0df3-649d-e053-2a95a90a0d0f2024-05-17WarningsExact identifier
spl id: 18a7d8ff-39bf-14fd-e063-6294a90a6182
spl set id: b9e248d7-0df3-649d-e053-2a95a90a0d0f

Reported adverse events (FAERS/openFDA)#

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