NANO PURE- benzalkonium chloride liquid

Nano Pure by

Drug Labeling and Warnings

Nano Pure by is a Otc medication manufactured, distributed, or labeled by Nano Global. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.10%

Purpose

Antiseptic

Uses

Helps reduce bacteria on skin that potentially cause disease.

Warnings

For external use only.

Do not use

in the eyes; if contact occurs, rinse thoroughly with water.

over large areas of the body.

if you are allergic to any ingredients.

Ask a doctor before use if you have

deep puncture wounds.

animal bites.

serious burns.

Stop use and ask a doctor if

condition persists or gets worse.

skin irritation or redness develop.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact Poison Control Center immediately.

Directions

Spray onto hands or skin and apply evenly until dry.

Other information

Store at 20° to 25°C (68° to 77°F) 

Inactive Ingredients

1-Octadecanaminium,N,N-dimethyl-N(3-(trihydroxysilyl)-propyl)-chloride, Ethyl Alcohol, Fragrance (Parfum), Purified Water.

Questions?

1-833-777-NANO

Principal Display Panel

nano™ PURE

Active Skin Protection

Patented Formula

Kills 99.99% of Germs

24 HOUR GERM BARRIER

Join the Nano™ movement and register today at MYNANO.COM

Long-Lasting

Most hand sanitizers only protect for seconds

Safe*

Nano Pure™ forms a safe germ barrier

*when used as directed

Protects

Kills 99.99% of germs

Be Well, Do Good

Your purchase supports the fight against infectious diseases worldwide

Dermatologist Tested

U.S. Pat. No. 6,613,755

Manufactured for

Nano Global Corp. Austin, TX 78701

MADE IN THE U.S.A.

INGREDIENTS AND APPEARANCE

NANO PURE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71530-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
1-OCTADECANAMINIUM, N,N-DIMETHYL-N-(3-(TRIHYDROXYSILYL)PROPYL) CHLORIDE (UNII: GLJ50K866T)
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71530-024-01	10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/26/2017
2	NDC: 71530-024-02	47.32 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/26/2017
3	NDC: 71530-024-03	236.59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/26/2017
4	NDC: 71530-024-04	800 mL in 1 BAG; Type 0: Not a Combination Product	06/26/2017
5	NDC: 71530-024-05	207 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/29/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/26/2017

Labeler - Nano Global (079594740)