Liquid Pro Hand Sanitizer Gel

Manufacturer: Saerom International, Inc.
Effective date: 2020-04-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:08:45

Label at a glance#

ProductLiquid Pro Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

• Hand sanitizer to decrease bacteria on the skin • Recommended for repeated use

Dosage and administration

• Rub thoroughly over all surfaces of both hands. • Rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• Hand sanitizer to decrease bacteria on the skin • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

keep out of eyes. In case of contact, flush eyes with water.

Stop use and consult a doctor if

OTC - STOP USE SECTION

irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• Rub thoroughly over all surfaces of both hands.
• Rub hands together briskly until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf extract, fragrance, hydroxyethylcellulose, propylene glycol, water

Package Labeling:75774-000-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Package Labeling:75774-000-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2360876	benzalkonium chloride 0.12 % Topical Gel	PSN	1
2360876	benzalkonium chloride 0.0012 MG/MG Topical Gel	SCD	1
2360876	benzalkonium chloride 0.12 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75774-000-01	2021-07-23	C162847	48780-1	c7ccaba7-0f54-fd44-e053-dadaa90aa01b	Liquid Pro Hand Sanitizer Gel
75774-000-02	2021-07-23	C162847	48780-1	c7ccaba7-0f54-fd44-e053-dadaa90aa01b	Liquid Pro Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75774-000-01	Liquid Pro Hand Sanitizer	3790 mL in 1 BOTTLE	GEL	3790		1
75774-000-02	Liquid Pro Hand Sanitizer	60 mL in 1 BOTTLE	GEL	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75774-000	LIQUID PRO HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [SAEROM INTERNATIONAL, INC.]	1	Legacy NDC, 2 package rows	20200430_4014a81e-8ddb-4058-9d9d-cd5f610a95ea.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Liquid Pro Hand Sanitizer
BENZALKONIUM CHLORIDE
ALOE VERA LEAF
HYDROXYETHYL CELLULOSE, UNSPECIFIED
PROPYLENE GLYCOL
WATER
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75774-000	75774-000-01, 75774-000-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
HYDROXYETHYL CELLULOSE, UNSPECIFIED	T4V6TWG28D	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a46f875b-8b03-6f80-e053-2995a90a8758			4014a81e-8ddb-4058-9d9d-cd5f610a95ea	2020-04-29	Warnings	Exact identifier spl id: a46f875b-8b03-6f80-e053-2995a90a8758 spl set id: 4014a81e-8ddb-4058-9d9d-cd5f610a95ea

Reported adverse events (FAERS/openFDA)#

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