Hand Sanitizer by Bevco, S. de R.L de C.V. / Miguel Angel Chavez Mejia / Bevco, S. de R.L. de C.V. Hand Sanitizer

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Bevco, S. de R.L de C.V., Miguel Angel Chavez Mejia, Bevco, S. de R.L. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER- alcohol liquid 
Bevco, S. de R.L de C.V.

----------

Hand Sanitizer

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
2. Glycerol (1.45% v/v).
3. Hydrogen peroxide (0.125% v/v).
4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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

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

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• 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 Label - Principal Display Panel

1000 mL NDC: 80220-111-21

500 mL NDC: 80220-111-22

250mL NDC: 80220-111-23

1125 mL NDC: 80220-111-24

60 mL NDC: 80220-111-25

3700 mL NDC: 80220-111-31

20 L NDC: 80220-111-32

2 mL NDC: 80220-111-41

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80220-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	1.45 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80220-111-21	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/07/2020
2	NDC: 80220-111-22	500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/07/2020
3	NDC: 80220-111-23	250 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/07/2020
4	NDC: 80220-111-24	125 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/07/2020
5	NDC: 80220-111-25	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/07/2020
6	NDC: 80220-111-31	3700 mL in 1 JUG; Type 0: Not a Combination Product	09/07/2020
7	NDC: 80220-111-32	20000 mL in 1 JUG; Type 0: Not a Combination Product	09/07/2020
8	NDC: 80220-111-41	2 mL in 1 POUCH; Type 0: Not a Combination Product	09/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/07/2020	01/31/2023

Labeler - Bevco, S. de R.L de C.V. (951582087)

Registrant - Miguel Angel Chavez Mejia (079852239)

Establishment
Name	Address	ID/FEI	Business Operations
Bevco, S. de R.L. de C.V.		951582087	manufacture(80220-111)

Revised: 12/2023

Document Id: 0cf77601-ed9b-f7b2-e063-6294a90a108c

34390-5

Set id: ad7dfb2d-35b8-1d7c-e053-2995a90affc9

Version: 2

Effective Time: 20231220