FDA.reportPublic FDA data

TerrasilMed Infection Control and Protection

Manufacturer
Aidance Skincare & Topical Solutions, LLC
Effective date
2023-05-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:30:49

Label at a glance#

ProductTerrasilMed Infection Control and Protection
Active ingredientALLANTOIN, BENZETHONIUM CHLORIDE
Label structure7 sections

Indications and uses

Helps protect skin and supports healing of minor cuts, scrapes, burns and wounds, including pressure sores, diabetic ulcers and cracked skin. Topical antiseptic to help decrease the risk of skin infection.

Dosage and administration

Wash and dry affected skin. Apply a thin layer of product. Cover affected area with a clean bandage. Repeat procedure as directed by healthcare provider or daily until affected area improves. Store at room temperature. May stain fabrics.

Label contents#

Full prescribing information#

Active Ingredients                                    Purpose

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.5%                                             Skin Protectant
Benzethonium Chloride 0.1%                        First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

Helps protect skin and supports healing of minor cuts, scrapes, burns and wounds, including pressure sores, diabetic ulcers and cracked skin. Topical antiseptic to help decrease the risk of skin infection.

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 or serious burns.

Keep out of reach of children. If swallowed, consult a physician.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash and dry affected skin. Apply a thin layer of product. Cover affected area with a clean bandage. Repeat procedure as directed by healthcare provider or daily until affected area improves. Store at room temperature. May stain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beeswax, MCT (coconut oil), Petrolatum, Silver Stearate, Sorbic Acid

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 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-02524909-025-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
YELLOW WAX2ZA36H0S2VIACT
COCONUT OILQ9L0O73W7LIACT
PETROLATUM4T6H12BN9UIACT
SILVER STEARATE4H6PCL92ZNIACT
SORBIC ACIDX045WJ989BIACT
ALLANTOIN344S277G0ZACTIB
BENZETHONIUM CHLORIDEPH41D05744ACTIB

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
193dd5e4-5b70-2e38-e063-6294a90a789e14b805c3-a016-4379-9620-cfb7642acfeb2024-05-24WarningsExact identifier
spl set id: 14b805c3-a016-4379-9620-cfb7642acfeb

Reported adverse events (FAERS/openFDA)#

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