BioMee Hand Sanitizer Lotion

BioMee Hand Sanitizer by

Drug Labeling and Warnings

BioMee Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by MC2 Therapeutics, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BIOMEE HAND SANITIZER- ethyl alcohol lotion 
MC2 Therapeutics 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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BioMee Hand Sanitizer Lotion

Drug Facts

Active ingredient

Ethyl Alcohol 83%

Purpose
Antiseptic

Uses

• hand sanitizer to help reduce bacteria on the skin that could potentially cause disease
• recommended for repeated use

Warnings
For external use only
Flammable, keep away from fire or flame

When using this product do not use in or near the eyes. In case of eye contact, rinse eyes with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• put enough product in your palm to cover hands and rub your hands briskly until dry
• children under 6 years of age should be supervised when using this product

Other information

• do not store above 105°F (40°C)
• may discolor certain fabrics and surfaces

Inactive ingredients

water, glycerin, mineral oil, isostearyl isostearate, carbomer copolymer type A (allyl pentaerythritol crosslinked), panthenol, edetol, povidone K30, polyoxyl 40 hydrogenated castor oil

Distributed by: MC2 Therapeutics Inc,

8 The Green, Dover, DE19901, USA

Made in France

biomee™

Hand Sanitizer Lotion

pad technology™

3.4 FL OZ (100 mL)

BIOMEE HAND SANITIZER 
ethyl alcohol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73499-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	83 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
PANTHENOL (UNII: WV9CM0O67Z)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
EDETOL (UNII: Q4R969U9FR)
POVIDONE K30 (UNII: U725QWY32X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73499-010-01	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/05/2020	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/05/2020	12/31/2022

Labeler - MC2 Therapeutics Ltd. (345388560)

Revised: 12/2022

Document Id: efade4fb-79ed-e85e-e053-2995a90a10f1

34390-5

Set id: a7572347-1032-61c8-e053-2995a90a4d2d

Version: 3

Effective Time: 20221212