LAFCO HAND SANITIZER BLUE MERCURY GRAPEFRUIT LAVENDER CUCUMBER- 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 Hand Sanitizer Blue Mercury Grapefruit Lavender Cucumber

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

Aqua(Water), Parfum(Fragrance), Glycerin, Aloe Barbadensis Leaf Juice, Acrylates/C10-30 AlkylAcrylateCrosspolymer, Triethanolamine, t-ButylAlcohol, PropyleneGlycol, Ethylene Brassylate, Citric Acid, Ginkgo Bioba Extract, Sodium Benzoate, Potassium Sorbate.

Package Labeling:380ml

Bottle

Package Labeling:100ml

Bottle2

LAFCO HAND SANITIZER BLUE MERCURY GRAPEFRUIT LAVENDER CUCUMBER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:77513-008
Route of Administration	TOPICAL

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:77513-008-38	380 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2021	04/09/2024
2	NDC:77513-008-10	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2021	12/03/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	04/01/2021	12/03/2024

Labeler - GFL SA (486270809)