RELIEF HAND SANITIZING WIPES- ethanol cloth 
Daehan P&H Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Relief HAND SANITIZING WIPES | 1 ct. in 1 packet < 20 ct. in 1 box | 79002-162-20

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

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 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

Relief HAND SANITIZING WIPES

RELIEF HAND SANITIZING WIPES 
ethanol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79002-162
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79002-162-2020 in 1 BOX06/22/2020
1NDC:79002-162-011 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/22/2020
Labeler - Daehan P&H Co., Ltd. (557818402)
Establishment
NameAddressID/FEIBusiness Operations
Sauber Co.,Ltd.690395844manufacture(79002-162)

Revised: 6/2020
Document Id: a8abb15d-cf56-29fc-e053-2a95a90ac18f
Set id: a8aba3bd-55b6-14d1-e053-2995a90a2a0f
Version: 1
Effective Time: 20200622
 
Daehan P&H Co., Ltd.