75 Alcohol Hand Sanitizing Wipes

75 Alcohol Hand Sanitizing Wipes by

Drug Labeling and Warnings

75 Alcohol Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by E-Fresh Food Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

75 ALCOHOL HAND SANITIZING WIPES- alcohol cloth 
E-Fresh Food 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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75 Alcohol Hand Sanitizing Wipes

Drug Facts

Active Ingredient

Ethyl alcohol 75% v/v

Purpose

Antiseptic

Uses

• Antibacterial (skin) cleanser. Kills harmful bacteria/germs.
• For personal hand hygiene to help prevent the spread of bacteria.

Warnings

For external use only.

When using this product,

avoid contact with eyes, If contact occurs, rinse thoroughly with water.

Stop use and ask / consult a doctor/ health care practitioner/health care provider / health care professional

if irritation develops.

KEEP OUT OF REACH OF CHILDREN.

If swallowed, call a poison control center or get medical help right away.

Directions

Adults and children over 2 years:
For occasional and personal domestic use Supervise children when they use this product. Wipe hands thoroughly. Let the skin dry and discard.

Other Information

Keep away from open flame and sources of heat.

Inactive Ingredients

Aloe barbadensis leaf extract, Water.

Questions?

Or report a serious adverse event,
Please call xxxxxxxxxxx (USA) XXXXXXXXX(CA)

Package Labeling:

Package Labeling:

75 ALCOHOL HAND SANITIZING WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80199-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80199-008-01	80 in 1 BAG	08/20/2020	10/30/2021
1		1.65 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 80199-008-02	80 in 1 BOX	09/29/2020	10/30/2021
2		1.71 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/20/2020	10/30/2021

Labeler - E-Fresh Food Ltd. (203413216)

Revised: 10/2021

Document Id: cea488f7-8040-8668-e053-2a95a90ad3fc

34390-5

Set id: ad66bad7-d3a8-0c8d-e053-2a95a90ab2f4

Version: 3

Effective Time: 20211018