UNCLE BUDS HAND SANITIZER- benzalkonium chloride liquid

Uncle Buds Hand Sanitizer by

Drug Labeling and Warnings

Uncle Buds Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by CBH International LLC, TAKA USA Inc. dba Cosmetic Innovations. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.1% w/w

Purpose

Antiseptic

Use

to decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

For external use only

When using this product

• Keep out of eyes. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

• Irritation or redness develops

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. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

Other Information

Store at room temperature. Avoid excessive heat.

Inactive Ingredients

Aloe Vera Leaf, Caesalpinia Spinosa Gum, Canola Oil, Diethylene Glycol Monoethyl Ether, Ethylhexylglycerin, Glycerin, Phenoxyethanol, Safflower Oil, Water

Questions?

Visit Unclebudshemp.com

Bottle Label

INGREDIENTS AND APPEARANCE

UNCLE BUDS HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72680-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAESALPINIA SPINOSA RESIN (UNII: WL3883U2PO)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CANOLA OIL (UNII: 331KBJ17RK)
SAFFLOWER OIL (UNII: 65UEH262IS)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72680-010-01	227 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/23/2020

Labeler - CBH International LLC (116834275)

Establishment
Name	Address	ID/FEI	Business Operations
TAKA USA Inc. dba Cosmetic Innovations		802860515	manufacture(72680-010)