Dove

Manufacturer: Conopco Inc. d/b/a/ Unilever
Effective date: 2024-11-07
Label type: HUMAN OTC DRUG LABEL
Version: 5
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.

Contacts and useful links#

PhoneLabel contact1-800-761-3683

Label contents#

Full prescribing information#

DOVE MEN +CARE SKIN DEFENSE BODY WASH - Benzalkonium Chloride

DESCRIPTION SECTION

Dove Men +Care Skin Defense 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 (Aqua), Sodium C12-13 Pareth Sulfate, Cocamidopropyl Betaine, Glycerin, Sodium Chloride, Fragrance (Parfum), Stearic Acid, Palmitic Acid, Citric Acid, Sodium Benzoate, Tetrasodium EDTA, PPG-9, Limonene, Linalool, Red 33 (CI 17200), Yellow 5 (CI 19140).

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-761-3683

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dove Men Skin Defense Body Wash

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	5
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	5
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	5
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-1836-1	2026-01-29	C162847	48780-1	49896155-b988-586f-e063-e6dba90add90	Dove Men +Care Skin Defense Body Wash
64942-1836-2	2026-01-29	C162847	48780-1	49896155-b988-586f-e063-e6dba90add90	Dove Men +Care Skin Defense Body Wash
64942-1836-3	2026-01-29	C162847	48780-1	49896155-b988-586f-e063-e6dba90add90	Dove Men +Care Skin Defense Body Wash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
64942-1836-1	Dove	532 mL in 1 BOTTLE	LIQUID	532	5
64942-1836-2	Dove	400 mL in 1 BOTTLE	LIQUID	400	5
64942-1836-3	Dove	887 mL in 1 BOTTLE	LIQUID	887	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-1836	DOVE (DOVE MEN PLUS CARE SKIN DEFENSE BODY WASH) LIQUID [CONOPCO INC. D/B/A/ UNILEVER]	5	Legacy NDC, 3 package rows	20241109_b9192b75-c8b2-3fe4-e053-2995a90a5ce4.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

Dove
Dove Men plus Care Skin Defense Body Wash
BENZALKONIUM CHLORIDE
BENZALKONIUM
D&C RED NO. 33
STEARIC ACID
SODIUM CHLORIDE
CITRIC ACID MONOHYDRATE
FD&C YELLOW NO. 5
WATER
GLYCERIN
LIMONENE, (+)-
PALMITIC ACID
EDETATE SODIUM
SODIUM BENZOATE
PPG-9
LINALOOL, (+/-)-
COCAMIDOPROPYL BETAINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-1836	64942-1836-1, 64942-1836-2, 64942-1836-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
D&C RED NO. 33	9DBA0SBB0L	IACT
STEARIC ACID	4ELV7Z65AP	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
LIMONENE, (+)-	GFD7C86Q1W	IACT
PALMITIC ACID	2V16EO95H1	IACT
EDETATE SODIUM	MP1J8420LU	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
PPG-9	I29VQH0G0B	IACT
LINALOOL, (+/-)-	D81QY6I88E	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2653506b-efc4-097b-e063-6394a90a9db2			b9192b75-c8b2-3fe4-e053-2995a90a5ce4	2024-11-07	Warnings	Exact identifier spl id: 2653506b-efc4-097b-e063-6394a90a9db2 spl set id: b9192b75-c8b2-3fe4-e053-2995a90a5ce4

Reported adverse events (FAERS/openFDA)#

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