LXR-Handy Andy Sanitizer Spray

Handy Andys by

Drug Labeling and Warnings

Handy Andys by is a Otc medication manufactured, distributed, or labeled by LXR Biotech LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HANDY ANDYS- hand sanitizer spray liquid 
LXR Biotech LLC

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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LXR-Handy Andy Sanitizer Spray

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 59-86F (15-30C)
Avoid freezing and excessive heat above 104F (40C)
May discolor certain fabrics or surfaces

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

57mL NDC: 78299-141-11

HANDY ANDYS 
hand sanitizer spray liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78299-141
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)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78299-141-12	57 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020	12/20/2022

Labeler - LXR Biotech LLC (117520926)

Establishment
Name	Address	ID/FEI	Business Operations
LXR Biotech LLC		968357405	manufacture(78299-141)

Revised: 12/2022

Document Id: f00ab92c-e66b-3ffc-e053-2995a90a2a36

34390-5

Set id: af4d422b-3330-32ca-e053-2995a90ae9e4

Version: 4

Effective Time: 20221217