TENA Barrier Cream

Manufacturer
Essity HMS North America Inc
Effective date
2022-01-25
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 22:11:53

Label at a glance#

ProductTENA Barrier Cream
Active ingredientDIMETHICONE
Label structure11 sections

Storage and handling

Other Information   Store between 32°F and 85°F

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Dimethicone 1.2%

OTC - PURPOSE SECTION

Purpose

Skin Protectant

INDICATIONS & USAGE SECTION

Uses

•protects skin from irritation casued by contact with urine and/or

stool  •helps prevent and releive chafed, chapped or cracked skin

WARNINGS SECTION

Warnings

For external use only.

Do not use •on deep or puncture wounds  •on animal bites

•on serious burns

When using this product  •do not get into eyes

Stop use and ask a doctor if  •condition worsens

•symptoms last more than 7 days or clear up and occur

again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical

help or contact a Poison Control Center immediately. 

DOSAGE & ADMINISTRATION SECTION

Directions

•cleanse skin with TENA® Cleansing Cream and/or TENA®

Washcloths  •apply cream liberally and reapply as needed

STORAGE AND HANDLING SECTION

Other Information  Store between 32°F and 85°F

INACTIVE INGREDIENT SECTION

Inactive Ingredients:  Acacia Decurrens

Flower Wax, Allantoin, Aloe Barbadensis Leaf Juice, Avena

Sativa (Oat) Kernel Flour, Behentrimonium Methosulfate,

Butylene Glycol, Calendula Officinalis Flower Oil, 

Caprylic/Capric Triglyceride, Cetearyl Alcohol, Cetyl Alcohol, 

Chamomilla Recutita (Matricaria) Flower Extract, Copernica

Cerifera (Carnauba) Wax, Distearyldimonium Chloride, 

Ethylhexylglycerin, Glycerin, Helianthus Annus (Sunflower)

Seed Wax, Hydrogenated Castor Oil, Isopropyl Palmitate, 

Jojoba Esters, Lactic Acid, Phenoxyethanol, Polyglycerin-3, 

Potassium Sorbate, Ricinus Communis (Castor) Seed Oil, 

Sodium Benzoate, Sodium Chloride, Sorbitan Caprylate, Water

OTC - QUESTIONS SECTION

Questions or comments? 

Call 1-800-992-9939 or visit www.tena.us

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59608-00559608-005-17, 59608-005-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Source Document#

Source XML · Source PDF

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
018e541a-09f5-592c-e063-6294a90a0a30fa28b1af-eda1-4549-9935-50e12717cd712023-07-28WarningsExact identifier
spl set id: fa28b1af-eda1-4549-9935-50e12717cd71

Reported adverse events (FAERS/openFDA)#

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