FDA.reportPublic FDA data

Nano Pure

Manufacturer
Nano Global
Effective date
2018-12-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:57:46

Label at a glance#

ProductNano Pure
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Indications and uses

• Helps reduce bacteria on skin that potentially cause disease.

Dosage and administration

•Spray onto hands or skin and apply evenly until dry.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• Helps reduce bacteria on skin that potentially cause disease.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

• 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

OTC - ASK DOCTOR SECTION

• deep puncture wounds.

• animal bites.

• serious burns.

Stop use and ask a doctor if

OTC - STOP USE SECTION

• condition persists or gets worse.

• skin irritation or redness develop.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

•Spray onto hands or skin and apply evenly until dry.

Other information

SPL UNCLASSIFIED SECTION

• Store at 20° to 25°C (68° to 77°F) 

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

1-833-777-NANO

Principal Display Panel

PACKAGE LABEL.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.

nano10mlnano10ml

nano1-6oznano1-6oz

nano8oznano8oz

nano800mlnano800ml

foamerfoamer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1052947benzalkonium chloride 0.1 % Topical SprayPSN4
1052947benzalkonium chloride 1 MG/ML Topical SpraySCD4
1052947benzalkonium chloride 0.1 % Topical SpraySY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71530-024-012020-01-31C16284748780-19d75b9d0-3fe8-f424-e053-dadaa90a57ceNano Pure
71530-024-022020-01-31C16284748780-19d75b9d0-3fe8-f424-e053-dadaa90a57ceNano Pure
71530-024-032020-01-31C16284748780-19d75b9d0-3fe8-f424-e053-dadaa90a57ceNano Pure
71530-024-042020-01-31C16284748780-19d75b9d0-3fe8-f424-e053-dadaa90a57ceNano Pure
71530-024-052020-01-31C16284748780-19d75b9d0-3fe8-f424-e053-dadaa90a57ceNano Pure

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71530-024-01Nano Pure10 mL in 1 BOTTLE, SPRAYLIQUID104
71530-024-02Nano Pure47.32 mL in 1 BOTTLE, SPRAYLIQUID47.324
71530-024-03Nano Pure236.59 mL in 1 BOTTLE, SPRAYLIQUID236.594
71530-024-04Nano Pure800 mL in 1 BAGLIQUID8004
71530-024-05Nano Pure207 mL in 1 BOTTLE, PUMPLIQUID2074

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71530-024NANO PURE (BENZALKONIUM CHLORIDE) LIQUID [NANO GLOBAL]4Legacy NDC, 5 package rows20181219_5624f334-98c6-401b-abf6-6d3892ea1eff.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71530-02471530-024-01, 71530-024-02, 71530-024-03, 71530-024-04, 71530-024-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
1-OCTADECANAMINIUM, N,N-DIMETHYL-N-(3-(TRIHYDROXYSILYL)PROPYL) CHLORIDEGLJ50K866TIACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
7ced0f7f-98db-d2f0-e053-2991aa0a13395624f334-98c6-401b-abf6-6d3892ea1eff2018-12-13WarningsExact identifier
spl id: 7ced0f7f-98db-d2f0-e053-2991aa0a1339
spl set id: 5624f334-98c6-401b-abf6-6d3892ea1eff

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.