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 ingredient

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

Ethyl Alcohol, Fragrance (Parfum), Purified Water.

Questions?

OTC - QUESTIONS SECTION

1-833-777-NANO

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NanoPure1

NanoPure2

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1038791	Benzalkonium (Topical)	benzalkonium chloride 1 MG/ML Topical Solution	SCD Active

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Nano Pure
Benzalkonium Chloride
ALCOHOL
WATER
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71530-025	71530-025-01, 71530-025-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b4e12b3c-8631-57d2-e053-2a95a90a86b1			a58ea3e7-8e53-3df1-e053-2995a90a58bc	2020-11-24	Warnings	Exact identifier spl set id: a58ea3e7-8e53-3df1-e053-2995a90a58bc

Reported adverse events (FAERS/openFDA)#

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

Nano Pure