FDA.reportPublic FDA data

Terrasil Burn Care and Relief maximum strength

Manufacturer
Aidance Skincare & Topical Solutions, LLC
Effective date
2020-11-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:04:14

Label at a glance#

ProductTerrasil Burn Care and Relief maximum strength
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 stain fabrics.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

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

Menthol 0.15% .........................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 physician.

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 stain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

beeswax (organic), bentonite (volcanic clay), cotton seed oil, eucalyptus citriodora oil, jojoba seed oil, magnesium oxide, peppermint oil, Silver Stearate, zinc oxide.

Questions?: 401-432-7750 or www.aidance.com

Product label

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 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-19324909-193-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZACTIB
MENTHOLL7T10EIP3AACTIB
WHITE WAX7G1J5DA97FIACT
BENTONITEA3N5ZCN45CIACT
COTTONSEED OILH3E878020NIACT
EUCALYPTUS OIL2R04ONI662IACT
JOJOBA OIL724GKU717MIACT
MAGNESIUM OXIDE3A3U0GI71GIACT
PEPPERMINT OILAV092KU4JHIACT
SILVER OXIDE897WUN6G6TIACT
ZINC OXIDESOI2LOH54ZIACT
STEARIC ACID4ELV7Z65APIACT

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
198d0708-a712-8870-e063-6394a90aa448f319b85b-fbbe-4d80-a63c-90538ae7705f2024-05-28WarningsExact identifier
spl set id: f319b85b-fbbe-4d80-a63c-90538ae7705f

Reported adverse events (FAERS/openFDA)#

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