Terrasil Burn Care and Relief

Manufacturer
Aidance Skincare & Topical Solutions, LLC
Effective date
2025-07-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:35:58

Label at a glance#

ProductTerrasil Burn Care and Relief
Active ingredientALLANTOIN, MENTHOL
Label structure6 sections

Indications and uses

For temporary relief of pain and itching due to minor burns, sunburn and skin irritations.

Dosage and administration

Apply directly to affected area. Do not use more than 4 times per day. Do not bandage damaged skin. Store at room temperature. May temporarily (washable) discolor skin and fabrics in sunlight.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.5%.........................Skin Protectant

Menthol 0.1% .........................Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of pain and itching due to minor burns, sunburn and skin irritations.

Warnings

WARNINGS SECTION

For external use only.

Avoid contact with eyes. Do not apply to open wounds or damaged skin.

If symptoms persist for more than seven days, discontinue use and consult physician.

If pregnant or breastfeeding, contact physician prior to use.

Keep out of reach of children. If swallowed, consult Poison Control.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply directly to affected area. Do not use more than 4 times per day. Do not bandage damaged skin. Store at room temperature. May
temporarily (washable) discolor skin and fabrics in sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

beeswax, cottonseed oil, eucalyptus oil, jojoba oil, magnesium oxide, peppermint oil, silver stearate, zinc oxide.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

terrasil Burn Care & Reliefterrasil Burn Care & Relief

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-19424909-194-50

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
39b13285-370c-b9b7-e063-6294a90aca9cc5b40f35-63a4-4f3d-b873-d514c47ce8992025-07-11WarningsExact identifier
spl id: 39b13285-370c-b9b7-e063-6294a90aca9c
spl set id: c5b40f35-63a4-4f3d-b873-d514c47ce899

Reported adverse events (FAERS/openFDA)#

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