HAND PROTECTOR- benzalkonium chloride solution

Hand Protector by

Drug Labeling and Warnings

Hand Protector by is a Otc medication manufactured, distributed, or labeled by Cytonix, LLC, Elaine Lanza. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride 0.13%

PURPOSE

Purpose: Antiseptic. Hand and skin sanitizer.

INDICATIONS & USAGE

USES: to reduce bacteria on skin that could cause disease. Recommended for repeat use.

WARNINGS

WARNINGS

For external use only.
Do not use in eyes.
When using this product avoid contact with eyes. In case of eye contact flush with water. Stop use and ask doctor if irritation and redness develop.
Keep out of reach of children.
If swallowed, get medical attention or contact a Poison Control Center.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

WHEN USING

Avoid contact with eyes. In case of eye contact flush with plenty of water.

STOP USE

Stop use and ask doctor if irritation or redness develop.

INACTIVE INGREDIENT

3-(trimethoxysilyl) Propyl Dimethyl Octadecyl Ammonium Chloride, Ethyl Alcohol, Water

DOSAGE & ADMINISTRATION

Apply liberally to hands and gently rub until dry. Reapply after 4 hours.

QUESTIONS

Contact:

Cytonix LLC, Beltsville, MD

20705 USA 301-470-6267

www.cytonix.com

PRINCIPAL DISPLAY PANEL

Hand Protector label 79291-653-03 16oz (473mL)

INGREDIENTS AND APPEARANCE

HAND PROTECTOR 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79291-653
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
WATER (UNII: 059QF0KO0R)	84 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79291-653-01	120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	07/01/2020
2	NDC: 79291-653-02	473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/31/2020
3	NDC: 79291-653-03	473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/01/2020

Labeler - Cytonix, LLC (831532705)

Registrant - Elaine Lanza (831532705)

Establishment
Name	Address	ID/FEI	Business Operations
Cytonix, LLC		831532705	manufacture(79291-653)