FDA.reportPublic FDA data

Devolver Clean Hand Tissue

Manufacturer
Devolver Cosmetics Co., Ltd
Effective date
2020-05-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:30:29

Label at a glance#

ProductDevolver Clean Hand Tissue
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping For children under 6, use only under adult supervision.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

DOSAGE & ADMINISTRATION SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age

on open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth.

In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

if irritation or rash occurs.

These may be signs of a serious condition.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

INDICATIONS & USAGE SECTION

Wet hands thoroughly with product and allow to dry without wiping

For children under 6, use only under adult supervision.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)

Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Hydroxy Acetophenone, Cetylpyridinium Chloride, Citric Acid, Butylene Glycol, Aloe ferox leaf extract, Fragrance (Lime)

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100g NDC: 75001-205-01 Label 1100g NDC: 75001-205-01 Label 1

100g NDC: 75001-205-01 Label 2100g NDC: 75001-205-01 Label 2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75001-20575001-205-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
LIME (CALCIUM OXIDE)C7X2M0VVNHIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
ALOE FEROX LEAF0D145J8EMEIACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

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
a5baeffb-f63a-e419-e053-2a95a90a1f10a5b8364e-1941-130b-e053-2995a90a70db2020-05-15WarningsExact identifier
spl id: a5baeffb-f63a-e419-e053-2a95a90a1f10
spl set id: a5b8364e-1941-130b-e053-2995a90a70db

Reported adverse events (FAERS/openFDA)#

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