FDA.reportPublic FDA data

T3 Wound Wash

Manufacturer
Patient Focused Telehealth
Effective date
2024-04-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:05:09

Label at a glance#

ProductT3 Wound Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Clean the affected area Apply a small amount of this product on the area 1 to 3 times daily Allow to dry Cover the affected area with sterile bandage if needed When bandaged, let dry first

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (0.1% by volume)

purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

First aid to help prevent infection in minor diabetic ulcers, pressure ulcers, cuts, scrapes and burns.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes

stop use and ask a doctor if

OTC - STOP USE SECTION

the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean the affected area
  • Apply a small amount of this product on the area 1 to 3 times daily
  • Allow to dry
  • Cover the affected area with sterile bandage if needed
  • When bandaged, let dry first

Other Information

OTHER SAFETY INFORMATION

Store at 40 to 120 F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

ascorbic acid, aloe barbadensis leaf juice, carbomer, cholecalciferol, citric acid, dimethyl sulfoxide, diazolidinyl urea, dipropylene glycol, dmdm hydantoin, glycerin, polysorbate 20, sodium dodecylbenzene sulfonate, tetrasodium EDTA, triethanolamine, tocopheryl acetate (vitamin E acetate), water

Questions

OTC - QUESTIONS SECTION

Tel. 800-918-7534 Email Address: info@patientfocusedtelehealth.com Manufactured by: TG Labs, LLC 7318 S Revere Pkwy, Centennial CO 80112 For: Patient focused tele-health LLC, 400 Country Ridge, Rockwall, TX USA 75087

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front PanelFront PanelT3 Wound Wash

Benzalkonium Chloride 0.1%

First Aid Antiseptic Solution

1 FL OZ 30 mL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72053-004-042024-04-17C16284748780-11030e365-4dbe-111a-e063-dadaa90a10e2T3 Wound Wash
72053-004-042024-01-30C16284748780-11030e365-4dbe-111a-e063-dadaa90a10e2T3 Wound Wash

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72053-00472053-004-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CHOLECALCIFEROL1C6V77QF41IACT
DIMETHYL SULFOXIDEYOW8V9698HIACT
DMDM HYDANTOINBYR0546TOWIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
SODIUM DODECYLBENZENESULFONATE554127163YIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
POLYSORBATE 207T1F30V5YHIACT
EDETATE SODIUMMP1J8420LUIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
DIPROPYLENE GLYCOLE107L85C40IACT

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
1f1c5208-8367-068d-e063-6294a90a1972e46ad070-f29b-2dbc-e053-2a95a90ae47e2024-08-07WarningsExact identifier
spl set id: e46ad070-f29b-2dbc-e053-2a95a90ae47e

Reported adverse events (FAERS/openFDA)#

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