Suave

Manufacturer: Conopco Inc. d/b/a/ Unilever
Effective date: 2022-08-31
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:50:35

Label at a glance#

ProductSuave

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

helps decrease bacteria on the hands

Dosage and administration

Wet hand thoroughly with product and rub lightly until dry. Do not wipe off or rinse

Contacts and useful links#

PhoneLabel contact1-800-782-8301

Websitewww.suave.com

www.suave.com

Label contents#

Full prescribing information#

SUAVE ESSENTIALS OCEAN BREEZE HAND SANITIZER - Ethyl Alcohol gel

DESCRIPTION SECTION

Suave Skin Solutions Hand Sanitizer Lotion

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 75.60%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

helps decrease bacteria on the hands

Warnings

WARNINGS SECTION

For external use only
Flammable. Keep away from fire or flame
Do not store in car.
Avoid contact with eyes, In case of contact, rinse eyes thoroughly with water.
If irritation develops, discontinue use and consult a doctor.

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 hand thoroughly with product and rub lightly until dry. Do not wipe off or rinse

Other information

OTHER SAFETY INFORMATION

• May discolor fabrics or surfaces.
• Store below 105˚F (40˚C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Fragrance (Parfum), Hydroxypropylcellulose, Lauryl Lactate, Myristyl Lactate, Cetyl Lactate, Cocos Nucifera (Coconut) Oil, Aloe Barbadensis Leaf Juice, Blue 1 (CI 42090) Red 33 (CI 17200).

Call

OTC - QUESTIONS SECTION

1-800-782-8301 or visit www.suave.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Suave Ocean Breeze Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2374568	ethanol 75.6 % Topical Gel	PSN	2
2374568	ethanol 0.756 ML/ML Topical Gel	SCD	2
2374568	ethanol 75.6 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-2043-1	2024-01-30	C162847	48780-1	1030e365-2190-111a-e063-dadaa90a10e2	Suave Essentials Ocean Breeze Hand Sanitizer
64942-2043-2	2024-01-30	C162847	48780-1	1030e365-2190-111a-e063-dadaa90a10e2	Suave Essentials Ocean Breeze Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64942-2043-1	Suave	236 mL in 1 BOTTLE	GEL	236		2
64942-2043-2	Suave	59 mL in 1 BOTTLE	GEL	59		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-2043	SUAVE (ESSENTIALS OCEAN BREEZE HAND SANITIZER) GEL [CONOPCO INC. D/B/A/ UNILEVER]	2	Legacy NDC, 2 package rows	20220901_e0756955-02e7-66ac-e053-2a95a90a86be.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

Suave
Essentials Ocean Breeze Hand Sanitizer
ALCOHOL
HYDROXYPROPYL CELLULOSE, UNSPECIFIED
LAURYL LACTATE
MYRISTYL LACTATE
WATER
GLYCERIN
COCONUT OIL
ALOE VERA LEAF
FD&C BLUE NO. 1
D&C RED NO. 33
CETYL LACTATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-2043	64942-2043-1, 64942-2043-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
HYDROXYPROPYL CELLULOSE, UNSPECIFIED	9XZ8H6N6OH	IACT
LAURYL LACTATE	G5SU0BFK7O	IACT
MYRISTYL LACTATE	1D822OC34X	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
COCONUT OIL	Q9L0O73W7L	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
CETYL LACTATE	A7EVH2RK4O	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
e78d6853-81bb-628d-e053-2995a90a6c56			e0756955-02e7-66ac-e053-2a95a90a86be	2022-08-31	Warnings	Exact identifier spl id: e78d6853-81bb-628d-e053-2995a90a6c56 spl set id: e0756955-02e7-66ac-e053-2a95a90a86be

Reported adverse events (FAERS/openFDA)#

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