DAB

Manufacturer: Three Kings Corp | Best Sanitizers, Inc
Effective date: 2020-02-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:03:42

Label at a glance#

ProductDAB

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

receive a small amount of foam into palm of hand rub thoroughly over all surfaces of both hands rub hands together until dry

Storage and handling

Store in a cool dry place below 104 F (40 C)

Contacts and useful links#

PhoneLabel contact888-872-2350

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin
Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product

Do not use in or near eyes

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, seek medical attention or contact Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

receive a small amount of foam into palm of hand
rub thoroughly over all surfaces of both hands
rub hands together until dry

Other information

STORAGE AND HANDLING SECTION

Store in a cool dry place below 104 F (40 C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, cocamidopropyl betaine, glycerin, poloxamer 124, phenoxyethanol, benzyl alcohol, dehydroacetic acid, sodium hydroxide, citric acid, D&C Green No. 8

Questions?

OTC - QUESTIONS SECTION

Contact Three Kings Corp. at 888-872-2350 Mon-Fri 9 am - 4pm CST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

dab

HAND PROTECTANT + SANITIZER

MICROBIOLOGICAL DEFENSE SPECTRUM

1.2L (1.26 QT) 40.5 GL OZ

dapprotects.com/healthcare

container labeBcontainer labelA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046310	benzalkonium chloride 0.12 % Topical Foam	PSN	1
1046310	benzalkonium chloride 1.2 MG/ML Topical Foam	SCD	1
1046310	benzalkonium chloride 0.12 % Topical Foam	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72898-001-01	2022-01-28	C162847	48780-1	d6a99b39-a081-a426-e053-dadaa90af4c2	9e42c2fb-0499-53ad-e053-2995a90a923c
72898-001-02	2022-01-28	C162847	48780-1	d6a99b39-a081-a426-e053-dadaa90af4c2	9e42c2fb-0499-53ad-e053-2995a90a923c
72898-001-03	2022-01-28	C162847	48780-1	d6a99b39-a081-a426-e053-dadaa90af4c2	9e42c2fb-0499-53ad-e053-2995a90a923c
72898-001-04	2022-01-28	C162847	48780-1	d6a99b39-a081-a426-e053-dadaa90af4c2	9e42c2fb-0499-53ad-e053-2995a90a923c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72898-001-01	DAB	45 mL in 1 BOTTLE, PUMP	SOLUTION	45	1
72898-001-02	DAB	250 mL in 1 BOTTLE, PUMP	SOLUTION	250	1
72898-001-03	DAB	1200 mL in 1 BOTTLE, PUMP	SOLUTION	1200	1
72898-001-04	DAB	946352 mL in 1 DRUM	SOLUTION	946352	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72898-001	DAB (BENZALKONIUM CHLORIDE) SOLUTION [THREE KINGS CORP]	1	Legacy NDC, 4 package rows	20200212_9e42c2fb-0499-53ad-e053-2995a90a923c.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

DAB
BENZALKONIUM CHLORIDE
GLYCERIN
PHENOXYETHANOL
DEHYDROACETIC ACID
CITRIC ACID MONOHYDRATE
BENZALKONIUM
BENZYL ALCOHOL
SODIUM HYDROXIDE
WATER
COCAMIDOPROPYL BETAINE
POLOXAMER 124
D&C GREEN NO. 8

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72898-001	72898-001-01, 72898-001-02, 72898-001-03, 72898-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
DEHYDROACETIC ACID	2KAG279R6R	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
BENZYL ALCOHOL	LKG8494WBH	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
POLOXAMER 124	1S66E28KXA	IACT
D&C GREEN NO. 8	I2W85YOX9L	IACT

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
9e42c2fb-049a-53ad-e053-2995a90a923c			9e42c2fb-0499-53ad-e053-2995a90a923c	2020-02-10	Warnings	Exact identifier spl id: 9e42c2fb-049a-53ad-e053-2995a90a923c spl set id: 9e42c2fb-0499-53ad-e053-2995a90a923c

Reported adverse events (FAERS/openFDA)#

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

DAB