FDA.reportPublic FDA data

Jabon Avena

Manufacturer
Industria La Popular, S.A.
Effective date
2023-06-21
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:29:43

Label at a glance#

ProductJabon Avena
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), Dimethicone, Butyrospermum Parkii (Shea Butter), Oatmeal Sativa Kernel Flour, Etidronic Acid, Titanium Dioxide, Prunus Amygdalus Dulcis (Sweet Almond) Oil

Questions

OTC - QUESTIONS SECTION

1-801-0026227 or atencionalcliente@ilpsa.com

Jabón DK12 Avena

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62476-10162476-101-38, 62476-101-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM PALM KERNELATE6H91L1NXTWIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
PRUNUS DULCIS BARK32F32E1WJJIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
DIMETHICONE92RU3N3Y1OIACT
ETIDRONIC ACIDM2F465ROXUIACT
OAT KERNEL OIL3UVP41R77RIACT
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES0C9AC7D6XUIACT

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
fea8244b-411b-614f-e053-6394a90a04ffa8486b9b-e0f1-2e0b-e053-2a95a90acda72023-06-21WarningsExact identifier
spl id: fea8244b-411b-614f-e053-6394a90a04ff
spl set id: a8486b9b-e0f1-2e0b-e053-2a95a90acda7

Reported adverse events (FAERS/openFDA)#

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