RELIEF HAND SANITIZING WIPES- ethanol cloth

Relief HAND SANITIZING WIPES by

Drug Labeling and Warnings

Relief HAND SANITIZING WIPES by is a Otc medication manufactured, distributed, or labeled by Daehan P&H Co., Ltd., Sauber Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethanol 62% Purpose: Antiseptic

Purpose

Antiseptic

Uses

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

Warnings

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

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

Directions

■ Remove the wipes one by one, and use on the skin gently.
■ 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.
■ Do not allow infants and toddlers swallow or put in the mouth.
■ 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

■ Store between 15-30°C (59-86ºF)

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

Inactive ingredients

Water, Glycerin

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

RELIEF HAND SANITIZING WIPES 
ethanol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79002-162
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79002-162-20	20 in 1 BOX	06/22/2020
1	NDC: 79002-162-01	1 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/22/2020

Labeler - Daehan P&H Co., Ltd. (557818402)

Establishment
Name	Address	ID/FEI	Business Operations
Sauber Co.,Ltd.		690395844	manufacture(79002-162)