Lafco New York Hand Sanitizer CHAMOMILE LAVENDER

Lafco New York Hand Sanitizer Chamomile Lavender by

Drug Labeling and Warnings

Lafco New York Hand Sanitizer Chamomile Lavender by is a Otc medication manufactured, distributed, or labeled by GFL SA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LAFCO NEW YORK HAND SANITIZER CHAMOMILE LAVENDER- alcohol gel 
GFL SA

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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Lafco New York Hand Sanitizer CHAMOMILE LAVENDER

Drug Facts

Active ingredient

Ethyl alcohol 73.2%

Purpose

Antiseptic

Use

for hand washing to decrease bacteria on the skin

Warnings

For external use only

Flammable, keep away from fire or flame.

Do not use

in the eyes

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet hands thoroughly with product and allow to dry without wiping.

Other information

• Store between 59-86°F (15-30°C)
• Avoid freezing and excessive heat above 104°F (40°C)

Inactive ingredients

Water (aqua), Parfum (fragrance), glycerin, aloe barbadensis leaf juice, acrylates/c-10-30 alkyl acrylate crosspolymer, triethanolamine, t-butyl alcohol, propylene glycol, ethylene brassylate, citric acid, ginkgo biloba extract, sodium benzoate, potassium sorbate.

Package Labeling:380ml

Package Labeling:100ml

LAFCO NEW YORK HAND SANITIZER CHAMOMILE LAVENDER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77513-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	73.2 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GINKGO (UNII: 19FUJ2C58T)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77513-006-01	380 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2021	03/19/2024
2	NDC: 77513-006-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2021	03/19/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2021	03/19/2024

Labeler - GFL SA (486270809)

Revised: 6/2022

Document Id: e1e5c588-d9e8-33b7-e053-2995a90ae634

34390-5

Set id: bb78670a-697f-5798-e053-2995a90aa32f

Version: 3

Effective Time: 20220620