Label at a glance#

ProductConsult Health Persistence Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Indications and uses

• For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use. • For wound sanitizing to help prevent bacterial contamination in cuts, scrapes, burns, lacerations and skin infections.

Dosage and administration

• Spray onto hands as needed. Pump onto hands as needed. Rub briskly together until dry. No rinsing required. • Pump onto wounds 3 times a day after cleaning. Allow foam to dissipate. Wipe excess with sterile gauze. May be bandaged once dry.

Contacts and useful links#

PhoneLabel contact1-866-272-4425

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial and First aid antiseptic

Uses:

INDICATIONS & USAGE SECTION

• For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use. • For wound sanitizing to help prevent bacterial contamination in cuts, scrapes, burns, lacerations and skin infections.

Warnings:

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush eyes with water.

Discontinue use if

SPL UNCLASSIFIED SECTION

irritation or redness develops. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

• Spray onto hands as needed. Pump onto hands as needed. Rub briskly together until dry. No rinsing required. • Pump onto wounds 3 times a day after cleaning. Allow foam to dissipate. Wipe excess with sterile gauze. May be bandaged once dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

ionized water, carbamide

Questions or Comments?

OTC - QUESTIONS SECTION

1-866-272-4425

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel2

Package Labeling: 97.59mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1020365	Benzalkonium (Topical)	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	5
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	5
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70803-004-02	2023-01-30	C162847	48780-1	f386c649-fa7f-0266-e053-dadaa90a7c1a	Consult Health Persistence Hand Sanitizer
70803-004-03	2023-01-30	C162847	48780-1	f386c649-fa7f-0266-e053-dadaa90a7c1a	Consult Health Persistence Hand Sanitizer
70803-004-09	2023-01-30	C162847	48780-1	f386c649-fa7f-0266-e053-dadaa90a7c1a	Consult Health Persistence Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70803-004-02	Consult Health Persistence Hand Sanitizer	59.15 mL in 1 BOTTLE, SPRAY	LIQUID	59.15	5
70803-004-03	Consult Health Persistence Hand Sanitizer	97.59 mL in 1 BOTTLE, SPRAY	LIQUID	97.59	5
70803-004-09	Consult Health Persistence Hand Sanitizer	264 mL in 1 BOTTLE, SPRAY	LIQUID	264	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70803-004	CONSULT HEALTH PERSISTENCE HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [GEO MANAGEMENT CORPORATION]	5	Legacy NDC, 3 package rows	20210724_8f1646af-8893-4e3e-b538-05d893daa9ce.zip

Products#

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

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

Consult Health Persistence Hand Sanitizer
BENZALKONIUM CHLORIDE
WATER
UREA
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70803-004	70803-004-09, 70803-004-03, 70803-004-02

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
WATER	059QF0KO0R	IACT
UREA	8W8T17847W	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
c7d1e1f9-b760-bf24-e053-2a95a90a6d09			8f1646af-8893-4e3e-b538-05d893daa9ce	2021-07-23	Warnings	Exact identifier spl id: c7d1e1f9-b760-bf24-e053-2a95a90a6d09 spl set id: 8f1646af-8893-4e3e-b538-05d893daa9ce

Reported adverse events (FAERS/openFDA)#

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

Consult Health Persistence Hand Sanitizer

Label at a glance#

Indications and uses

Dosage and administration

Contacts and useful links#

Label contents#

Full prescribing information#

Active ingredient

Purpose

Uses:

Warnings:

When using this product

Discontinue use if

Keep out of reach of children.

Directions:

Inactive ingredients

​Questions or Comments?

Package Labeling:

Package Labeling: 97.59mL

Package Labeling:

Related RxNorm Concepts#

DailyMed RxNorm Mappings#

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

DailyMed Dashboard NDC Coverage#

Products#

NDC Codes#

Ingredients#

Source Document#

openFDA label cross-check#

Reported adverse events (FAERS/openFDA)#

Questions or Comments?