Hand Hero Hand Sanitizer by United Laboratories Manufacturing, LLC Hand Hero Hand Sanitizer

Hand Hero Hand Sanitizer by

Drug Labeling and Warnings

Hand Hero Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by United Laboratories Manufacturing, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND HERO HAND SANITIZER- alcohol gel 
United Laboratories Manufacturing, LLC

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Hand Hero Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl Alcohol 70.0% v/v

Purpose

Anti-Microbial

Uses

• Hand Sanitizer helps reduce bacteria on the skin that could cause disease.
• Recommended for repeated use.

Warnings

Flammable: Keep away from excessive heat or open flame.For external use only

When using this product

• Avoid contact with eyes. In case of eye contact flush with water.
• Do not apply to open wounds or damaged skin.

Keep out of reach of children.

• If accidentally swallowed or ingested, get medical help or contact poison control center immediately.
• Do not drink. Not edible. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Stop use and ask a doctor if

• Rash or irritation develops and lasts.
• If condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days.

Directions

• Apply entire packet to palm of hand 
• Use no water or towels.
• Rub until hands are completely covered
• Agitate lightly until dry
• Do not rinse or wipe with towel.

Other Information

Storage

• Do not store above 105 F.
• May discolor some fabrics.
• Harmful to wood finishes and plastics.

Inactive Ingredients

Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Carbomer, Water.

Questions or Comments?

Visit www.handhero.com

Package Labeling:

HAND HERO HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62400-0004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62400-0004-1	50 in 1 BOX	05/07/2020	11/30/2021
1		2.25 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/07/2020	11/30/2021

Labeler - United Laboratories Manufacturing, LLC (807878116)

Establishment
Name	Address	ID/FEI	Business Operations
United Laboratories Manufacturing, LLC		807878116	manufacture(62400-0004) , label(62400-0004) , pack(62400-0004)

Revised: 2/2024

Document Id: 113372a4-58da-f829-e063-6294a90a4eb1

34390-5

Set id: cbd38fcd-c952-46a2-b6c5-a394da82e32c

Version: 4

Effective Time: 20240212