Hand Sanitizer Wipes by DIGITAL ALLY, INC. Hand Sanitizer Wipes

Hand Sanitizer Wipes by

Drug Labeling and Warnings

Hand Sanitizer Wipes by is a Otc medication manufactured, distributed, or labeled by DIGITAL ALLY, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER WIPES- alcohol cloth 
DIGITAL ALLY, INC.

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

Drugs Facts

Active Ingredient: [s]

Alcohol 75% (v/v)

Purpose

Antiseptic

Use[s]

Alcohol Sanitizer Wipe to help reduce bacteria/germs that potentially can cause disease.

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.

Directions

• Open bag and use for hands.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

• Store between 15-30C (59-86F).
• Avoid freezing and excessive heat above 40C (104F).

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP.

Package Labeling:

Package Labeling:100 Sheets

HAND SANITIZER WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81192-289
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
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81192-289-25	25 in 1 BAG	10/01/2020	12/01/2022
1		5 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 81192-289-10	100 in 1 CANISTER	01/20/2021	01/01/2022
2		5 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	10/01/2020	12/01/2022

Labeler - DIGITAL ALLY, INC. (612961933)

Revised: 7/2022

Document Id: e3c90983-d7fe-0f9d-e053-2a95a90ae673

34390-5

Set id: b5e5776e-06c9-21f5-e053-2995a90afae2

Version: 3

Effective Time: 20220714