Suave HAND SANITIZER

Manufacturer
UNILEVER ASIA PRIVATE LIMITED
Effective date
2020-06-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:25:14

Label at a glance#

ProductSuave HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

help decrease bacteria on the hands

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

help decrease bacteria on the hands

Warnings

WARNINGS SECTION

For exteral 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 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 hands thoroughly with product and rub lightly until dry. Do not wipe off or rinse.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aminomethyl Propanol, Carbomer,Denatonium Benzoate, Purified Water USP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Suave 500mL_Sinno01b LBL_Suave 500mL_Sinno

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50069-10650069-106-06, 50069-106-16
75497-103

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
2eea19e6-ed73-3030-e063-6294a90a1808bf80fb6c-2b60-42a1-b6ef-b661334dcb832025-02-24WarningsExact identifier
spl set id: bf80fb6c-2b60-42a1-b6ef-b661334dcb83

Reported adverse events (FAERS/openFDA)#

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