FDA.reportPublic FDA data

Suave

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:52:14

Label at a glance#

ProductSuave
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

help decrease bacteria on the hands

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. Rub lightly until dry. Do not rinse.

Label contents#

Full prescribing information#

SUAVE HAND SANITIZER - Ethyl Alcohol liquid

DESCRIPTION SECTION

Suave Hand Sanitizer

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 75.6%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

help decrease bacteria on the hands

Warnings

WARNINGS SECTION

• For external use only
• Flammable. Keep away from fire or flame
• Avoid contact with eyes, in case of contact, rinse eyes thoroughly with water immediately.
• If irritation develps, 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 hands thoroughly with product and allow to dry without wiping. Rub lightly until dry. Do not rinse.

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cetyl Lactate, Glycerin, Hydroxypropylcellulose, Lauryl Lactate, Myristyl Lactate, Water (Aqua)

Questions?

OTC - QUESTIONS SECTION

Call us at 1-800-782-8301.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SuaveHandSanitizerSuaveHandSanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1491797ethanol 76 % Topical SolutionPSN4
1491797ethanol 0.76 ML/ML Topical SolutionSCD4
1491797ethanol 76 % Topical SolutionSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1736-12024-01-30C16284748780-11030e365-0641-111a-e063-dadaa90a10e2Suave Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1736-1Suave354 mL in 1 CONTAINERLIQUID3544

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1736SUAVE (ALCOHOL) LIQUID [CONOPCO INC. D/B/A/ UNILEVER]4Legacy NDC, 1 package rows20221208_a3fd52d8-ccf0-3418-e053-2995a90a3d40.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-173664942-1736-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETYL LACTATEA7EVH2RK4OIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
LAURYL LACTATEG5SU0BFK7OIACT
MYRISTYL LACTATE1D822OC34XIACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT

Source Document#

Source XML · Source PDF

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
ef406ee4-eab5-1eef-e053-2a95a90a2d87a3fd52d8-ccf0-3418-e053-2995a90a3d402022-12-07WarningsExact identifier
spl id: ef406ee4-eab5-1eef-e053-2a95a90a2d87
spl set id: a3fd52d8-ccf0-3418-e053-2995a90a3d40

Reported adverse events (FAERS/openFDA)#

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