LECHAT- hand sanitizer gel gel

LECHAT by

Drug Labeling and Warnings

LECHAT by is a Otc medication manufactured, distributed, or labeled by Mega Creation Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 60% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria.

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

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

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

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

Directions

• Wet hands thoroughly with the product and rub into the skin till 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

Purified Water, IsopiopylAlcohol, Hydrogen Peroxide, Glycerin, Isopropyl Myristate, Acrylates/C10-30 Ally Acrylate Crosspolymer, Aminomethyl Propanol, Cocoyl Caprylocaprate, Aloe Barbadensis Leaf Extract, Tocopheryl-acetate, fragrance, Lavender Oil, Orange Oil, Grapefruit Oil

Package Label - Principal Display Panel

51 mL NDC: 77857-832-01

INGREDIENTS AND APPEARANCE

LECHAT 
hand sanitizer gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77857-832
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
LAVENDER OIL (UNII: ZBP1YXW0H8)
GRAPEFRUIT OIL (UNII: YR377U58W9)
FRAGRANCE GREEN APPLE ORC2001072 (UNII: U9GH30P956)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
ORANGE OIL (UNII: AKN3KSD11B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77857-832-01	51 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2021
2	NDC: 77857-832-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2021
3	NDC: 77857-832-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/17/2021

Labeler - Mega Creation Inc. (014096208)

Registrant - Mega Creation Inc. (014096208)

Establishment
Name	Address	ID/FEI	Business Operations
Mega Creation Inc.		014096208	manufacture(77857-832)