HYDROCLEAN HAND SANITIZER- benzalkonium chloride 0.13% aerosol, foam

HydroClean Hand Sanitizer by

Drug Labeling and Warnings

HydroClean Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Telebrands Corp, Neutraderm, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13% w/w

Purpose

Benzalkonium Chloride 0.13% w/w....................Antiseptic

Uses

Antiseptic cleansing of hands and body to decrease bacteria on skin without soap and water.

Warnings

For external use only

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of eye contact, flush eyes with water.

Stop use and ask doctor if

• irritation or rash occurs. These might be signs of a serious condition.
• 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

• Apply a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands for 15 seconds. Allow hands to dry without wiping.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store tightly in a cool dry place.

Inactive ingredients

Water/Aqua/Eau, Glycerin, Decyl Glucoside, Hemp Seed Oil, Cocos Nucifera (Coconut) Oil, Aloe Barbadensis Leaf Extract, Sodium Hyaluronate, Phenoxyethanol, Sodium Citrate, Ethylhexylglycerin, Citric Acid, Disodium EDTA, Sodium Hydroxide

Questions?

Call (855) 877-4503 (M-F, 9am-5pm EST)

PRINCIPAL DISPLAY PANEL

Handvana

Odor Free

HydroClean

Hand Sanitizer

Benzalkonium Chloride 0.13%

KILLS 99.9% OF GERMS*

fast acting foam technology

Sanitize + Soften Hands

With Moisturizing

Coconut Oil

Aloe Vera

Hyaluronic Acid

7 fl oz (207 mL)

Synthesized in the USA

INGREDIENTS AND APPEARANCE

HYDROCLEAN HAND SANITIZER 
benzalkonium chloride 0.13% aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73287-008
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 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
COCONUT OIL (UNII: Q9L0O73W7L)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
WATER (UNII: 059QF0KO0R)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73287-008-01	1 in 1 CARTON	04/08/2020
1		207 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/08/2020

Labeler - Telebrands Corp (177266558)

Establishment
Name	Address	ID/FEI	Business Operations
Neutraderm, Inc.		146224444	manufacture(73287-008)