FDA.reportPublic FDA data

DK12 Vitamin E Antibacterial and Moisturizing

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 00:40:13

Label at a glance#

ProductDK12 Vitamin E Antibacterial and Moisturizing
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

For washing to decrease bacteria on the skin.

Dosage and administration

Wet bar with water Lather vigorously and wash skin Rinse and dry thoroughly

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

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. In case of eye contact, flush with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation and redness develops

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 bar with water
Lather vigorously and wash skin

Rinse and dry thoroughly

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium Palm Kernelate, Water, Glycerin, Fragrance (Perfume), Sodium Polyacrylate, Zea May Starch, Butyrospermum Parkii (Shea Butter), Etidronic Acid, Titanium Dioxide, Tocopheryl Acetate, Cocos Nucitera (coconut) oil, FD&C Yellow No. 5, FD&C Yellow No. 6.

Questions

OTC - QUESTIONS SECTION

1-801-0026227 or atencionalcliente@ilpsa.com

Dk12 Fresh Energy Bar Soap Antibacterial + Moisturizing

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabelboxbox

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
07cba15c-4adc-1039-9ab9-45f5b7e84f4fProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62476-107-15DK12 Vitamin E Antibacterial and Moisturizing140 g in 1 CELLO PACKSOAP1402
62476-107-42DK12 Vitamin E Antibacterial and Moisturizing420 g in 1 CELLO PACKSOAP4202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62476-107DK12 VITAMIN E ANTIBACTERIAL AND MOISTURIZING (BENZALKONIUM CHLORIDE 0.1%) SOAP [INDUSTRIA LA POPULAR, S.A.]2Current NDC, 2 package rows20241204_fe9270c0-bf6b-f0ff-e053-6394a90ae8f1.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62476-10762476-107-42, 62476-107-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
SODIUM PALM KERNELATE6H91L1NXTWIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
SODIUM POLYACRYLATE (8000 MW)285CYO341LIACT
ETIDRONIC ACIDM2F465ROXUIACT
STARCH, CORNO8232NY3SJIACT
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES0C9AC7D6XUIACT
COCONUT OILQ9L0O73W7LIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C YELLOW NO. 6H77VEI93A8IACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DK12 Vitamin E Antibacterial and MoisturizingBENZALKONIUM CHLORIDE 0.1%Industria La Popular, S.A.fe9270c0-bf6b-f0ff-e053-6394a90ae8f12024-12-02WarningsExact identifier
ndc (package): 62476-107-15
ndc (package): 62476-107-42
ndc (product): 62476-107
ndc11 (package): 62476010742
ndc11 (package): 62476010715
spl id: 284c61e7-5ad7-6ca9-e063-6294a90a29bc
spl set id: fe9270c0-bf6b-f0ff-e053-6394a90ae8f1

Reported adverse events (FAERS/openFDA)#

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