WET WIPES- ethyl alcohol swab
Zhejiang Qimei Commodity 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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69821-003 70% Alcohol Wet Wipes

Active ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

●For hand sanitizing to decrease bacteria on the skin
●Recommended for repeated use

Warnings

. FOR EXTERNAL USE ONLY
. FLAMMABL E, KEEP AWAY FROM FIRE OR FL AME
●When using this product avoid contact with eyes. In case of eye contact,
flush eyes with water and seek medical help.
●If swallowed drink large amounts of water and seek medical attention.
●Avoid contact with face and broken skin. If contact occurs, flush with water.
●Stop use and ask a doctor if rritation or redness develops

Note Do not store above00°F. Non-stainingMay discolor some fabrics.

Keep out of reach of children

Keep out of reach of children.

Directions

●Take wipe and rub thoroughly over all surfaces of both hands
●Allow to dry without wiping
●Dispose of wipe in trash after use. Do not flush.

Purfied Water, Anionic Surfactant,
Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice.

WET WIPES
ethyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69821-003
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:69821-003-01	10 in 1 PACKAGE	04/20/2020
1		2.5 g in 1 POUCH; Type 0: Not a Combination Product
2	NDC:69821-003-02	20 in 1 PACKAGE	04/20/2020
2		2.5 g in 1 POUCH; Type 0: Not a Combination Product
3	NDC:69821-003-03	30 in 1 PACKAGE	04/20/2020
3		2.5 g in 1 POUCH; Type 0: Not a Combination Product
4	NDC:69821-003-04	50 in 1 PACKAGE	04/20/2020
4		2.5 g in 1 POUCH; Type 0: Not a Combination Product
5	NDC:69821-003-05	80 in 1 PACKAGE	04/20/2020
5		2.5 g in 1 POUCH; Type 0: Not a Combination Product
6	NDC:69821-003-06	100 in 1 BAG	04/20/2020
6		2.5 g in 1 POUCH; Type 0: Not a Combination Product
7	NDC:69821-003-07	160 in 1 BAG	04/20/2020
7		0.48 g in 1 POUCH; Type 0: Not a Combination Product
8	NDC:69821-003-09	135 in 1 PAIL	04/20/2020
8		0.48 g in 1 POUCH; Type 0: Not a Combination Product
9	NDC:69821-003-08	1200 in 1 BAG	04/20/2020
9		0.47 g in 1 POUCH; Type 0: Not a Combination Product
10	NDC:69821-003-10	250 in 1 PAIL	04/20/2020
10		0.48 g in 1 POUCH; Type 0: Not a Combination Product
11	NDC:69821-003-11	1500 in 1 PAIL	04/20/2020
11		0.48 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/20/2020

Labeler - Zhejiang Qimei Commodity Co.,Ltd. (544331136)

Registrant - Zhejiang Qimei Commodity Co.,Ltd. (544331136)

Name	Address	ID/FEI	Business Operations
Establishment
Zhejiang Qimei Commodity Co.,Ltd.		544331136	manufacture(69821-003)