Relief HAND SANITIZING WIPE

Manufacturer
Daehan P&H Co., Ltd. | Sauber Co.,Ltd.
Effective date
2020-06-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:32

Label at a glance#

ProductRelief HAND SANITIZING WIPE
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

■ Tear open packet. Open and unfold wipe. Thoroughly wipe hands. ■ There is a risk of contamination if the wet wipe is put back into the packaging with unclean hands. ■ Do not throw away wipes in a flush toilet, as there is a risk of clogging it. ■ Supervise children under 6 years of age when using this product to avoid swallowing. ■ Avoid direct inhalation of vapors during application. (Headaches and irritation t...

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol 62% Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of
contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of
a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children If swallowed, get medical help or contact a
Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Tear open packet. Open and unfold wipe. Thoroughly wipe hands.

■ There is a risk of contamination if the wet wipe is put back into

the packaging with unclean hands.

■ Do not throw away wipes in a flush toilet, as there is a risk of clogging it.

■ Supervise children under 6 years of age when using this product to avoid

swallowing.

■ Avoid direct inhalation of vapors during application. (Headaches and
irritation to mucous membranes may occur when directly inhaled.)

■ Keep product in its original container as storing the product in anything
other than the original container may result in accidents or cause the integrity
of the product to diminish.

Other information

STORAGE AND HANDLING SECTION

■ Store between 15-30°C (59-86ºF)

■ Avoid freezing and excessive heat above 40°C (104ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Relief HAND SANITIZING WIPERelief HAND SANITIZING WIPE

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79002-062-012023-01-30C16284748780-1f386c64a-0604-0266-e053-dadaa90a7c1aRelief HAND SANITIZING WIPE | 1 individual sheet registration | 79002-062-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79002-062-01Relief HAND SANITIZING WIPE1 in 1 PACKETCLOTH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79002-062RELIEF HAND SANITIZING WIPE (ETHANOL) CLOTH [DAEHAN P&H CO., LTD.]1Legacy NDC, 1 package rows20200622_a8a69794-11ff-49f0-e053-2a95a90aab17.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79002-06279002-062-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
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
a8a6b0cc-371d-6df8-e053-2a95a90ade6aa8a69794-11ff-49f0-e053-2a95a90aab172020-06-22WarningsExact identifier
spl id: a8a6b0cc-371d-6df8-e053-2a95a90ade6a
spl set id: a8a69794-11ff-49f0-e053-2a95a90aab17

Reported adverse events (FAERS/openFDA)#

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