HAND SANITIZER WIPES by Zhejiang Qimei Cosmetics Co., Ltd. HAND SANITIZER WIPES

HAND SANITIZER WIPES by

Drug Labeling and Warnings

HAND SANITIZER WIPES by is a Otc medication manufactured, distributed, or labeled by Zhejiang Qimei Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER WIPES- alcohol wipes cloth 
Zhejiang Qimei Cosmetics 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 WIPES

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

to decrease bacteria on the skin that could cause disease

Warnings

For external use only: hands

Flammable. Keep away from fire and flame.

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin
do not inhale or ingest

Stop use and ask a doctor if

irritation or redness develops
condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet hands thoroughly with product and allow to dry

not recommended for infants

other information

do not store above 105ºF
may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

Aloe barbadensis leaf juice, glycerin, isopropanol, propanediol, tocopheryl acetate, water

Uses

to decrease bacteria on the skin that could cause disease

recommended for repeated use

Directions

wet hands thoroughly with product and allow to dry without wiping
not recommended for infants

20 WIPES, NDC: 81773-001-01

20 WIPES Label

160 WIPES, NDC: 81773-001-03

160 WIPES Label

50 WIPES, NDC: 81773-001-02

50 WIPES Label

HAND SANITIZER WIPES 
alcohol wipes cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 81773-001
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
WATER (UNII: 059QF0KO0R)  
PROPANEDIOL (UNII: 5965N8W85T)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 81773-001-0120 in 1 PACKAGE04/30/2021
11.32 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2NDC: 81773-001-0250 in 1 CANISTER04/30/2021
22.55 mL in 1 APPLICATOR; Type 0: Not a Combination Product
3NDC: 81773-001-03160 in 1 CANISTER04/30/2021
31.2 mL in 1 APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/30/2021
Labeler - Zhejiang Qimei Cosmetics Co., Ltd. (709887693)
Registrant - Zhejiang Qimei Cosmetics Co., Ltd. (709887693)
Establishment
NameAddressID/FEIBusiness Operations
Zhejiang Qimei Cosmetics Co., Ltd.709887693manufacture(81773-001)

Revised: 4/2021
Document Id: bfe55d1c-4934-653e-e053-2a95a90adee3
Set id: bfe55d1c-4933-653e-e053-2a95a90adee3
Version: 1
Effective Time: 20210428