HYDROCLEAN HAND SANITIZER (MAX)- benzalkonium chloride 0.13% gel

HydroClean Hand Sanitizer (Max) by

Drug Labeling and Warnings

HydroClean Hand Sanitizer (Max) 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 gel 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 closed in a cool dry place.

Inactive ingredients

Water/Aqua/Eau, Aloe Barbadensis Leaf Juice, Sodium Hyaluronate, Cocos Nucifera (Coconut) Oil, Cannabis Sativa (Hemp) Seed Oil, Hydroxyethylcellulose, Polysorbate 20, Disodium EDTA, Sodium Citrate, Sodium Hydroxide, Citric Acid, Blue 1 (CI 42090), Yellow 5 (CI 19140)

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*

Sanitize + Soften Hands

With Moisturizing

Coconut Oil

Aloe Vera

Hyaluronic Acid

VALUE SIZE

OVER 1lb

17 fl oz (503 mL)

MADE IN USA FROM GLOBALLY SOURCED INGREDIENTS

INGREDIENTS AND APPEARANCE

HYDROCLEAN HAND SANITIZER (MAX) 
benzalkonium chloride 0.13% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73287-009
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
SODIUM CITRATE (UNII: 1Q73Q2JULR)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
COCONUT OIL (UNII: Q9L0O73W7L)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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: 73287-009-01	1 in 1 CARTON	04/13/2020
1		503 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	04/13/2020

Labeler - Telebrands Corp (177266558)

Establishment
Name	Address	ID/FEI	Business Operations
Neutraderm, Inc.		146224444	manufacture(73287-009)