Nano Pure

Manufacturer
Nano Global
Effective date
2020-09-25
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:30:14

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 15° to 30°C (59° to 86°F). Avoid freezing and excessive heat above 40°C (104°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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

026-01026-01

71530.026.0271530.026.02

71530.026.0371530.026.03

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
71530-026-012022-01-28C16284748780-1d6a99b39-628c-a426-e053-dadaa90af4c2Nano Pure
71530-026-022022-01-28C16284748780-1d6a99b39-628c-a426-e053-dadaa90af4c2Nano Pure
71530-026-032022-01-28C16284748780-1d6a99b39-628c-a426-e053-dadaa90af4c2Nano Pure

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71530-026-01Nano Pure47.32 mL in 1 BOTTLE, SPRAYLIQUID47.324
71530-026-02Nano Pure59.15 mL in 1 BOTTLE, SPRAYLIQUID59.154
71530-026-03Nano Pure1249190 mL in 1 TANKLIQUID12491904

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71530-026NANO PURE (BENZALKONIUM CHLORIDE) LIQUID [NANO GLOBAL]4Legacy NDC, 3 package rows20200926_a7ea32b2-cd7f-9b52-e053-2a95a90af75a.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
71530-02671530-026-01, 71530-026-02, 71530-026-03

Ingredients#

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

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

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
b02a4e2a-392c-3387-e053-2995a90adddea7ea32b2-cd7f-9b52-e053-2a95a90af75a2020-09-25WarningsExact identifier
spl id: b02a4e2a-392c-3387-e053-2995a90addde
spl set id: a7ea32b2-cd7f-9b52-e053-2a95a90af75a

Reported adverse events (FAERS/openFDA)#

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