HAND SANITIZER- hand sanitizer spray 
Guangzhou BEAVER Cosmetic 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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HAND SANITIZER CLEANSING HAND SPRAY

Active Ingredient

Alcohol 80%v/v

Purpose

Antiseptic

Use

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 or flame.

Do not use

in children less than 2 months of age

on open skin wounds

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

Spray enough product on hands to cover all surfaces.Rub hands together until dry.

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

Other information

Store between 15-30(59-86)

Avoid freezing and excessive heat above 40(104)

Inactive ingredients

Water,Glycerin, Hydrogen Peroxide

Package Label - Principal Display Panel

60 ml label 100 ml label 200 ml label 60 ml label 100 m label 200 ml label 60 ml label 100 ml label 200 ml label

HAND SANITIZER 
hand sanitizer spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74159-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74159-004-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
2NDC:74159-004-02100 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
3NDC:74159-004-03200 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
4NDC:74159-004-0460 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
5NDC:74159-004-05100 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
6NDC:74159-004-06200 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
7NDC:74159-004-0760 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
8NDC:74159-004-08100 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
9NDC:74159-004-09200 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/26/2020
Labeler - Guangzhou BEAVER Cosmetic Co.,Ltd. (420020595)
Registrant - Guangzhou BEAVER Cosmetic Co.,Ltd. (420020595)
Establishment
NameAddressID/FEIBusiness Operations
Guangzhou BEAVER Cosmetic Co.,Ltd.420020595manufacture(74159-004)

Revised: 5/2020
Document Id: a68acba4-1241-24e1-e053-2a95a90a7a9c
Set id: a68a7e39-b724-dcc7-e053-2995a90aeeaa
Version: 1
Effective Time: 20200526
 
Guangzhou BEAVER Cosmetic Co.,Ltd.