FDA.reportPublic FDA data

Welly Clean Hands

Manufacturer
Welly Health PBC
Effective date
2021-12-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:19:42

Label at a glance#

ProductWelly Clean Hands
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For handwashing to decrease bacteria on skin without soap and water Recommended for repeated use

Dosage and administration

Wet hands & wrists thoroughly with product and allow to dry without wiping Children under 6 years of age should be supervised while using this product

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 66.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on skin without soap and water
  • Recommended for repeated use

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use in eyes. If this happens, rinse thoroughly with water

Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all drugs out of the reach of children. If ingested get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands & wrists thoroughly with product and allow to dry without wiping
  • Children under 6 years of age should be supervised while using this product

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

SPL UNCLASSIFIED SECTION

OINTMENT REFILLS

Welly FIRST AID  Clean Hands INSTANT HAND SANITIZER

Ethyl Alcohol

Get the refills you need to build the Welly first aid kits you want.

Keep hands clean when there's no sink in sight.

Distributed by: Welly Health PBC

Minneapolis, MN 55402

1-833-BE-WELLY

Welly TM     www.GetWelly.com

Made in U.S.A

RE19SAF

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
72663-11272663-112-23, 72663-112-12

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
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
D&C GREEN NO. 58J6RDU8L9XIACT
D&C YELLOW NO. 1035SW5USQ3GIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB

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
2cdd4d43-e4c8-b06c-e063-6294a90a61928fa74774-8eeb-4061-ba5d-e65914fc146f2025-01-29WarningsExact identifier
spl set id: 8fa74774-8eeb-4061-ba5d-e65914fc146f

Reported adverse events (FAERS/openFDA)#

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