PROFESSIONAL SOLUTIONS - HAND SANITIZER FOAM- benzalkonium chloride liquid

Professional Solutions - Hand Sanitizer Foam by

Drug Labeling and Warnings

Professional Solutions - Hand Sanitizer Foam by is a Otc medication manufactured, distributed, or labeled by Cosmetic Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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DRUG FACTS:

ACTIVE INGREDIENTS

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

USES

To decrease bacteria on the skin

WARNINGS

For external use only: Hands only

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Avoid contact with broken skin.

Stop use and seek a doctor if redness or irritation develops and persist 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 - for children under 6, use only under adult supervision - not recommended for infants.

INACTIVE INGREDIENTS

Water (Aqua), Propanediol, Glycereth-7 Triacetate, Glycerin, Babassu Oil Glycereth-8 Esters, Decyl Glucoside, Calendula Officinalis Flower Extract, Equisetum Arvense Extract, Geranium Maculatum Extract, Honey, Citric Acid, Panax Ginseng Root Extract, Salvia Officinalis Leaf Extract, Sambucus Nigra Flower Extract, Ethylhexylglycerin, Phenoxyethanol, Sodium Hydroxide.

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Manufactured By: Professional Solutions
Boca Raton, FL 33487

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Label

Professional
Solutions®
PURE SCIENCE. BETTER SKIN

hand sanitizer
foam

protect + moisturize

1.7 fl. oz. (50mL)

INGREDIENTS AND APPEARANCE

PROFESSIONAL SOLUTIONS - HAND SANITIZER FOAM 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66163-1900
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Propanediol (UNII: 5965N8W85T)
Glycereth-7 Triacetate (UNII: S9W6Z48HUP)
Glycerin (UNII: PDC6A3C0OX)
Babassu Oil Glycereth-8 Esters (UNII: 12XQ76K0YL)
Decyl Glucoside (UNII: Z17H97EA6Y)
Calendula Officinalis Flower (UNII: P0M7O4Y7YD)
Equisetum Arvense Branch (UNII: 1L0VKZ185E)
Geranium Maculatum Root (UNII: 93IXI5B6OJ)
Honey (UNII: Y9H1V576FH)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Asian Ginseng (UNII: CUQ3A77YXI)
Sambucus Nigra Flower (UNII: 07V4DX094T)
Ethylhexylglycerin (UNII: 147D247K3P)
Phenoxyethanol (UNII: HIE492ZZ3T)
Sodium Hydroxide (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66163-1900-0	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020
2	NDC: 66163-1900-1	120 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	05/01/2020

Labeler - Cosmetic Solutions LLC (807907928)