ALCOHOL WET WIPE- alcohol wet wipe gel 
HAND SANITIZER- hand sanitizer gel gel 
Guangzhou Daieme 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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Main active ingredient

70%(v/v) ethanol

Scope of application

Hands cleaning and disifection

Usage

for hands disinfection, take out about 2ml of gel, rub it on the skin for 1 minute, it can be dry without washing. Repeated use make a slight sticky feeling, please wash with water.

Notice

Flammable, please keep it away from fire.Please store it in an environment below 50℃.external used, don'ttake it by mouth, and don't contact with the eyes directly, once contacting with eyes,please wash eyes with plenty of clean water quickly. Please close it well after use to avoid volatilization.Take caution if you are allergic to alcohol.

Do not use

Flammable, please keep it away from fire.Please store it in an environment below 50°c.external used, don'ttake it by mouth, and don't contact with the eyes directly, once contacting with eyes,please wash eyes with plenty of clean water quickly. Please close it well after use to avoid volatilization.Take caution if you are allergic to alcohol.

Take caution if you are allergic to alcohol.

Keep our of reach of children. Avoid contacting with eyes, and damaged skin

Directions

Avoid contacting with eyes, and damaged skin

Other information

ingredients

water, EDTA disodium, carbomer, triethanolamine, ethyl alcohol.

Package label

gel labelWipes label

ALCOHOL WET WIPE 
alcohol wet wipe gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54237-031
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL72.7 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET) 0.5 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX) 1 mL  in 100 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54237-031-011 mL in 1 BAG; Type 0: Not a Combination Product03/30/2020
2NDC:54237-031-028 mL in 1 BAG; Type 0: Not a Combination Product03/30/2020
3NDC:54237-031-0310 mL in 1 BAG; Type 0: Not a Combination Product03/30/2020
4NDC:54237-031-0420 mL in 1 BAG; Type 0: Not a Combination Product03/30/2020
5NDC:54237-031-0525 mL in 1 BAG; Type 0: Not a Combination Product03/30/2020
6NDC:54237-031-0648 mL in 1 BAG; Type 0: Not a Combination Product03/30/2020
7NDC:54237-031-0750 mL in 1 BAG; Type 0: Not a Combination Product03/30/2020
8NDC:54237-031-0880 mL in 1 BAG; Type 0: Not a Combination Product03/30/2020
9NDC:54237-031-09100 mL in 1 BAG; Type 0: Not a Combination Product03/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/30/2020
HAND SANITIZER 
hand sanitizer gel gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54237-030
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
TROLAMINE (UNII: 9O3K93S3TK) 0.28 mL  in 100 mL
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) 0.01 mL  in 100 mL
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) 0.28 mL  in 100 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54237-030-012 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
2NDC:54237-030-0230 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
3NDC:54237-030-0360 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
4NDC:54237-030-0499 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
5NDC:54237-030-05100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
6NDC:54237-030-06120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
7NDC:54237-030-07300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
8NDC:54237-030-08500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
9NDC:54237-030-091000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
10NDC:54237-030-1029.57 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
11NDC:54237-030-11118.28 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
12NDC:54237-030-12236.56 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
13NDC:54237-030-13473.12 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/30/2020
Labeler - Guangzhou Daieme Cosmetic Co,.Ltd (542359812)
Establishment
NameAddressID/FEIBusiness Operations
Guangzhou Daieme Cosmetic Co,.Ltd542359812manufacture(54237-030, 54237-031)

Revised: 2/2021
Document Id: ba57b72f-9561-9fb0-e053-2995a90a7ae5
Set id: ba57b72f-956f-9fb0-e053-2995a90a7ae5
Version: 1
Effective Time: 20210202
 
Guangzhou Daieme Cosmetic Co,.Ltd