HAND SANITIZER- benzalkonium chloride soap

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by GREENERWAYS LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE

PURPOSE

ANTISEPTIC

USES

FOR HAND WASHING TO REDUCE BACTERIA ON SKIN.

WARNINGS

FOR ESTERNAL USE ONLY.

WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.

STOP USE AND ASK A DOCTOR IF IRRITATION AND REDNESS DEVELOP.

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.

(1-800-222-1222)

DIRECTIONS

PUMP INTO DRY HANDS. LATHER VIGOROUSLY FOR AT LEAST 15 SECONDS. RINSE AND DRY THOROUGHLY.

INACTIVE INGREDIENTS

WATER (AQUA), SODIUM C14-16 OLEFIN SULFONATE, COCAMIDOPROPYL HYDROXYSULTAINE, ALOE BARBADENSIS LEAF JUICE, SODIUM COCOYL ISETHIONATE, SODIUM PCA, PROPYLENE GLYCOL, GLYCERIN, COCAMIDE MIPA, ZINC GLUCONATE, POLYQUATERNIUM-10, PANTHENOL, COPPER GLUCONATE, CITRIC ACID

QUESTIONS?

1-800-777-1603

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74487-102
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)
SODIUM C14 OLEFIN SULFONATE (UNII: N816E2SOKI)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
PANTHENOL (UNII: WV9CM0O67Z)
COPPER GLUCONATE (UNII: RV823G6G67)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74487-102-15	480 mL in 1 POUCH; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - GREENERWAYS LLC (012436209)

Registrant - GREENERWAYS LLC (012436209)