RAW SPIRIT - MOISTURIZING HAND SANITIZER FOAM- benzalkonium chloride liquid

Raw Spirit - Moisturizing Hand Sanitizer Foam by

Drug Labeling and Warnings

Raw Spirit - Moisturizing 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]

SPL UNCLASSIFIED SECTION

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 ask a doctor if irritation or redness develops - 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 - 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.

PRINCIPAL DISPLAY PANEL - 120 ml Bottle Label

RAW
SPIRIT

moisturizing
antimicrobial
foam

4.1 fl. oz | 120ml

INGREDIENTS AND APPEARANCE

RAW SPIRIT - MOISTURIZING HAND SANITIZER FOAM 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66163-1901
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: 66163-1901-1	120 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	06/01/2020

Labeler - Cosmetic Solutions LLC (807907928)