Skindurance

Manufacturer
Skindure, LLC
Effective date
2015-04-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:47:06

Label at a glance#

ProductSkindurance
Active ingredientDIMETHICONE
Label structure10 sections

Indications and uses

• Helps prevent and temporarily protects and helps relieve chafed, chapped or cracked skin. • Helps protect from the drying effects of wind and cold weather.

Dosage and administration

• Apply as needed

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Dimethicone (1%)

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

• Helps prevent and temporarily protects and helps relieve chafed, chapped or cracked skin.

• Helps protect from the drying effects of wind and cold weather.

Warnings

WARNINGS SECTION

For external use only.  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.  Do not use on • deep or puncture wounds • animal bites • serious burns.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply as needed

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Caprylic/Capric Triglycerides, C18-36 Acid Triglycerides, Tribehenin, Aloe Barbadensis Leaf Extract, Jojoba Wax, Allantoin, Tocopheryl Acetate, Retinyl Palmitate, Hamamelis Virginiana (Witch Haxel) Leaf Extract

Other Information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

Questions or Comments?

OTC - QUESTIONS SECTION

Call 301-247-9677

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront LabelBack LabelBack Label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIMETHICONE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69802-025-012021-07-23C16284748780-1c7ccaba7-15cc-fd44-e053-dadaa90aa01bSkindurance

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69802-025-01Skindurance7090 mg in 1 APPLICATORSTICK70901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69802-025SKINDURANCE (DIMETHICONE) STICK [SKINDURE, LLC]1Legacy NDC, 1 package rows20160915_e802d881-4522-4879-b6c4-e127c8e625d0.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69802-02569802-025-01

Ingredients#

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

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

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
53f7aeff-0fb1-4b4a-8c18-06f0a77e12aae802d881-4522-4879-b6c4-e127c8e625d02015-04-30WarningsExact identifier
spl id: 53f7aeff-0fb1-4b4a-8c18-06f0a77e12aa
spl set id: e802d881-4522-4879-b6c4-e127c8e625d0

Reported adverse events (FAERS/openFDA)#

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