FRESHORIZE ALCOHOL FREE FOAMING HAND SANITIZER- benzalkonium chloride lotion

Freshorize Alcohol Free Foaming Hand Sanitizer by

Drug Labeling and Warnings

Freshorize Alcohol Free Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Freshorize Ltd, Freshorize USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Uses:

To decrease bacteria on the skin.

Warnings

For external use only.

Do not use in eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor is skin irritation develops.

If ingested, get medical help or contact a Poison Control Center immediately.

Warnings:

Keep out of reach of children.

Directions:

Liberally apply product to sin by gently massaging until absorbed.
Supervise children in the use of this product.

Other Information:

Avoid extreme temperatures.

Inactive Ingredients:

Water (Aqua), PEG-40 Hydrogenated Castor Oil, Parfum, Aloe Barbadensis Leaf Extract

Drug Facts

Active Ingredients
Benzalkonium Chloride

Purpose

Antibacterial.

Product / Brand Name Label

Freshorize Alcohol Free Hand Sanitizer

Requires no water or towels.
Apply small amounts to hands and rub lightly until dry.

www.freshorize.com

INGREDIENTS AND APPEARANCE

FRESHORIZE ALCOHOL FREE FOAMING HAND SANITIZER 
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52305-600
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
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)	0.75 g  in 100 mL
DMDM HYDANTOIN (UNII: BYR0546TOW)	0.2 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	3 g  in 100 mL
WATER (UNII: 059QF0KO0R)	95.07 g  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.1 g  in 100 mL

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52305-600-10	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/15/2020
2	NDC: 52305-600-20	280 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/15/2020
3	NDC: 52305-600-27	270 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/15/2020
4	NDC: 52305-600-25	250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/15/2020
5	NDC: 52305-600-16	160 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/15/2020
6	NDC: 52305-600-24	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/15/2020

Labeler - Freshorize Ltd (424168503)

Registrant - Freshorize USA LLC (078206924)