Lyrall TM LAVENDER ANTIBACTERIAL LIQUID HAND SOAP

Lyrall by

Drug Labeling and Warnings

Lyrall by is a Otc medication manufactured, distributed, or labeled by Mekor LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LYRALL ANTIBACTERIAL LAVENDER LIQUID HANDSOAP- benzalkonium chloride liquid 
Mekor 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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Lyrall TM LAVENDER ANTIBACTERIAL LIQUID HAND SOAP

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

For handwashing to decrease the bacteria on the skin.

Warnings

For External Use Only
When using the product Avoid contact with eyes. In case of eye contact, flush with water.
Stop use and ask a doctor if irritation or rash occurs.

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

Directions:

Pump into hands, wet as needed Lather vigorously for at least 20 seconds. Wash skin, rinse thoroughly and dry

Inactive ingredients:

Aqua (Water, Eau), Disodium EDTA, Glycerin, Sodium Lauryl Ether Sulfate, Cocamide MEA, Cocamidopropyl Betaine, Aloe Barbadensis Leaf Extract, Methylisothiazolinone and Methylchloroisothiazolinone, Lavandula Angustifolia (Lavender Flower) Oil, Citric Acid, Sodium Chloride, Fragrance and CI 17200 (Red 33) and CI 42090 (Blue).

Questions?

1-888-495-3978

KILLS 99.9% OF BACTERIA

WITH ALOE VERA & ESSENTIAL OILS

Moisturizing

Paraben Free & pH Balanced

Gentle Cleanser

Distributed by:
Mekor Corp
One Rockefeller Plaza, 11th Floor
New York, NY 10020
www.lyrall.com

Packaging

LYRALL  ANTIBACTERIAL LAVENDER LIQUID HANDSOAP
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77679-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
LAVENDER OIL (UNII: ZBP1YXW0H8)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77679-101-50	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/09/2020	02/28/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/09/2020	02/28/2023

Labeler - Mekor LLC (962457250)

Revised: 12/2021

Document Id: abaf0e9b-1416-4d20-8539-f0f9e080a24a

34390-5

Set id: 98ff8000-789b-49a5-961e-3decb3bb61e8

Version: 2

Effective Time: 20211215