Suave

Manufacturer
Midway Importing, Inc.
Effective date
2020-06-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:23:58

Label at a glance#

ProductSuave
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

help decrease bacteriaon the hands

Dosage and administration

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

Storage and handling

May discolor fabrics or surfaces. Store below 95°F(35℃)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol (80% v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

help decrease bacteriaon 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 develops, discontinue use and consult a doctor.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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.

Other information

STORAGE AND HANDLING SECTION

May discolor fabrics or surfaces. Store below 95°F(35℃)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aminomethyl Propanol, Carbomer, Denatonium Benzoate, Purified Water USP

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76095-019-162025-02-24C16284748780-1d6a99b39-75dd-a426-e053-dadaa90af4c2Suave Hand Sanitizer 80 sinno
76095-019-162022-01-28C16284748780-1d6a99b39-75dd-a426-e053-dadaa90af4c2Suave Hand Sanitizer 80 sinno

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
76095-01976095-019-16

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
2eea3933-09af-4237-e063-6294a90aa91ea93cf57f-8f4b-dda5-e053-2995a90a8f0d2025-02-24WarningsExact identifier
spl set id: a93cf57f-8f4b-dda5-e053-2995a90a8f0d

Reported adverse events (FAERS/openFDA)#

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