FDA.reportPublic FDA data

Dove

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-11-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:35:55

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

Dispense into hands, wash cloth or pouf, work into lather and use all over body. Rinse clean.

Label contents#

Full prescribing information#

DOVE CARE & PROTECT MOISTURE RENEW ANTIBACTERIAL BODY WASH - Benzalkonium Chloride

DESCRIPTION SECTION

Dove Care & Protect Moisture Renew Antibacterial Body Wash

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

Dispense into hands, wash cloth or pouf, work into lather and use all over body. Rinse clean.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Chloride, Cocamidopropyl Betaine, Sodium Lauroyl Glycinate, Sodium Lauroyl Isethionate, Acrylates Copolymer, Lauric Acid, Glycerin, Fragrance (Parfum), Phenoxyethanol, Glycol Distearate, Stearic Acid, Palmitic Acid, Tetrasodium EDTA, PEG-150 Pentaerythrityl Tetrastearate, PPG-2 Hydroxyethyl Cocamide, Helianthus Annuus (Sunflower) Seed Oil, Iodopropynyl Butylcarbamate, Citric Acid, Geraniol, Limonene, Linalool.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-761-3683

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DoveAntibacterialBodyWashDoveAntibacterialBodyWash

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN3
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD3
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY3
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1843-12026-01-29C16284748780-149896155-ab71-586f-e063-e6dba90add90Dove Care & Protect Moisture Renew Antibacterial Body Wash
64942-1843-22026-01-29C16284748780-149896155-ab71-586f-e063-e6dba90add90Dove Care & Protect Moisture Renew Antibacterial Body Wash
64942-1843-32026-01-29C16284748780-149896155-ab71-586f-e063-e6dba90add90Dove Care & Protect Moisture Renew Antibacterial Body Wash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1843-1Dove650 mL in 1 BOTTLELIQUID6503
64942-1843-2Dove710 mL in 1 BOTTLELIQUID7103
64942-1843-3Dove1000 mL in 1 BOTTLELIQUID10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1843DOVE (CARE AND PROTECT MOISTURE RENEW ANTIBACTERIAL BODY WASH) LIQUID [CONOPCO INC. D/B/A/ UNILEVER]3Legacy NDC, 3 package rows20241109_b9b90d9e-9b08-420e-e053-2a95a90aac5e.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-184364942-1843-1, 64942-1843-2, 64942-1843-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
SODIUM LAUROYL ISETHIONATEM590021Z02IACT
STEARIC ACID4ELV7Z65APIACT
SODIUM CHLORIDE451W47IQ8XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LIMONENE, (+)-GFD7C86Q1WIACT
PALMITIC ACID2V16EO95H1IACT
EDETATE SODIUMMP1J8420LUIACT
SUNFLOWER OIL3W1JG795YIIACT
SODIUM LAUROYL GLYCINATEL54QIO80PNIACT
GERANIOLL837108USYIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCOL DISTEARATE13W7MDN21WIACT
LAURIC ACID1160N9NU9UIACT
PEG-150 PENTAERYTHRITYL TETRASTEARATE8L4OOQ76AMIACT
PPG-2 HYDROXYETHYL COCAMIDE34N07GUJ3XIACT
LINALOOL, (+/-)-D81QY6I88EIACT

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
265356ec-cd0d-ef86-e063-6394a90ad332b9b90d9e-9b08-420e-e053-2a95a90aac5e2024-11-07WarningsExact identifier
spl id: 265356ec-cd0d-ef86-e063-6394a90ad332
spl set id: b9b90d9e-9b08-420e-e053-2a95a90aac5e

Reported adverse events (FAERS/openFDA)#

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