EDELWEISS INSTANT HAND SANITIZER- alcohol gel 
Guangdong Xuerou Industry 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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Edelweiss Instant Hand Sanitizer

Drug Facts

Active ingredient[s]

alcohol 75%

Purpose

Antiseptic

Use[s]

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

Other Information

Inactive ingredients

purified water, carbomer, parfum, aminomethyl propanol, aloe barbadensis leaf extract

Package Labeling:100ml

Label

Package Labeling:250ml

Label2

Package Labeling:500ml 79120-001-04

Label4Bottle8887

Package Labeling:500ml 79120-001-03

Label3Bottle8726

EDELWEISS INSTANT HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79120-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79120-001-01100 mL in 1 BOTTLE; Type 0: Not a Combination Product02/25/2020
2NDC:79120-001-02250 mL in 1 BOTTLE; Type 0: Not a Combination Product02/25/2020
3NDC:79120-001-03500 mL in 1 BOTTLE; Type 0: Not a Combination Product02/25/2020
4NDC:79120-001-04500 mL in 1 BOTTLE; Type 0: Not a Combination Product02/25/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/25/2020
Labeler - Guangdong Xuerou Industry Co., Ltd. (544793409)

Revised: 7/2020
Document Id: a9f158e1-5462-771d-e053-2a95a90aee2d
Set id: bac3172a-bf79-450e-a16a-862bd3886197
Version: 1
Effective Time: 20200708
 
Guangdong Xuerou Industry Co., Ltd.