DK12 Liquid Hand Creamy

Manufacturer: Industria La Popular, S.A.
Effective date: 2024-12-02
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:39:58

Label at a glance#

ProductDK12 Liquid Hand Creamy

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

For washing to decrease bacteria on the skin

Dosage and administration

Wet hands. Apply palmful to hands. Scrub thoroughly. Rinse thoroughly.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For External Use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

irritation or redness develops - condition persists for more than 72 hours.

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

Wet hands. Apply palmful to hands. Scrub thoroughly. Rinse thoroughly.

Other Information

OTHER SAFETY INFORMATION

Store between 15-30C (59-86F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Methylcloroisothiazolinone/Methylisothiazolinone, Sodium Benzotriazolyl Butylphenol Sulfonate/Buteth-3/Tributyl Citrate, FD&C Red No. 40, FD&C Yellow No. 5.

DK12 Liquid Hand Soap Creamy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	2
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	2
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	2
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62476-008-08	DK12 Liquid Hand Creamy	237 mL in 1 BOTTLE	LIQUID	237		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62476-008	DK12 LIQUID HAND CREAMY (BENZALKONIUM CHLORIDE 0.13%) LIQUID [INDUSTRIA LA POPULAR, S.A.]	2	Current NDC, 1 package rows	20241204_01e2e51b-212b-368e-e063-6294a90a871c.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

DK12 Liquid Hand Creamy
Benzalkonium Chloride 0.13%
SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE
BUTETH-3
METHYLCHLOROISOTHIAZOLINONE
TRIBUTYL CITRATE
BENZALKONIUM CHLORIDE
BENZALKONIUM
FD&C RED NO. 40
FD&C YELLOW NO. 5
METHYLISOTHIAZOLINONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62476-008	62476-008-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE	0LA2QC9O3Z	IACT
BUTETH-3	OC116GRO69	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
TRIBUTYL CITRATE	827D5B1B6S	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
FD&C RED NO. 40	WZB9127XOA	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	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
DK12 Liquid Hand Creamy	BENZALKONIUM CHLORIDE 0.13%	Industria La Popular, S.A.	01e2e51b-212b-368e-e063-6294a90a871c	2024-12-02	Warnings	Exact identifier ndc (package): 62476-008-08 ndc (product): 62476-008 ndc11 (package): 62476000808 spl id: 284c64c5-0ea7-05f1-e063-6394a90af987 spl set id: 01e2e51b-212b-368e-e063-6294a90a871c

Reported adverse events (FAERS/openFDA)#

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