RELIEF HAND SANITIZING WIPE- 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 WIPE | 1 individual sheet registration | 79002-062-01

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

■ 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

■ 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 WIPE

RELIEF HAND SANITIZING WIPE 
ethanol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79002-062
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:79002-062-011 in 1 PACKET; Type 0: Not a Combination Product06/22/2020
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(79002-062)

Revised: 6/2020
Document Id: a8a6b0cc-371d-6df8-e053-2a95a90ade6a
Set id: a8a69794-11ff-49f0-e053-2a95a90aab17
Version: 1
Effective Time: 20200622
 
Daehan P&H Co., Ltd.