FDA.reportPublic FDA data

Super T

Manufacturer
Dermal Source, Inc. | HTO Nevada, Inc. (dba Kirkman)
Effective date
2023-10-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:19:23

Label at a glance#

ProductSuper T
Active ingredientLidocaine Hydrochloride, Tetracaine Hydrochloride, Benzocaine
Label structure9 sections

Storage and handling

Other information:  Discard after expiration date. Store in cool, dark place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active Ingredient  (in each cc) Purpose
Lidocaine HCl   5% Topical Anesthetic
Tetracaine HCl   1% Topical Anesthetic
Benzocaine 12% Topical Anesthetic

INDICATIONS & USAGE SECTION

Uses: External Use Only on Intact Skin. Temporarily relives pain due to tattooing, makeup or other pain sensitive procedures.

WARNINGS SECTION

WARNINGS: Keep out of children's reach.
Keep out of eyes and mouth. In case of accidental contact with eyes, rinse immediately with copious amounts of eyewash. Seek care by an eye care physician. If accidently swallowed, get medical help immediately.

OTC - DO NOT USE SECTION

Do not use:

  • If you have a history of severe liver disease or impairment.
  • If you have a known allergy or sensitivity to any of the components of this product. If sensitivity occurs, discontinue use and seek medical attention as needed. If condition worsens or does not improve in seven days, or clears up and occurs again with a few days, discontinue use of the product and consult a doctor. Do not use in large quantities, particularly over raw surfaces or blistered areas.
  • If pregnant or nursing.

DOSAGE & ADMINISTRATION SECTION

Directions:  Sensitivity test advised prior to use.

Apply sparingly to affected area for 15-30 minutes. Remove and cleanse skin. Repeat as needed up to three times a day. Remove product before continuing with procedure.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Purified Water, Propylene Glycol, Ethyoxydiglycol, NF Emulsifying Wax, Polyacrylamide, Hydroxyethylcellulose, Diazolidinyl Urea, Methylparaben, Propylparaben, and EDTA.

STORAGE AND HANDLING SECTION

Other information: Discard after expiration date. Store in cool, dark place.

OTC - QUESTIONS SECTION

Questions? Contact distributor on product label.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TOP SHELF

SUPER
T

7/8 oz. 

topical anesthetic for use before
a pain sensitive procedure

Distributed by: DERMAL SOURCE
Portland, OR 97232

www.dermalsource.com
1-866-568-3223

label
label

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80069-01080069-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
Lidocaine HydrochlorideV13007Z41AACTIR
Tetracaine Hydrochloride5NF5D4OPCIACTIB
BenzocaineU3RSY48JW5ACTIB
Water059QF0KO0RIACT
Propylene Glycol6DC9Q167V3IACT
Diethylene Glycol Monoethyl EtherA1A1I8X02BIACT
White Wax7G1J5DA97FIACT
Diazolidinyl UreaH5RIZ3MPW4IACT
MethylparabenA2I8C7HI9TIACT
PropylparabenZ8IX2SC1OHIACT
Edetic Acid9G34HU7RV0IACT

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
cb4b1773-d71a-4676-8099-2fa4610e3550be7fc3d4-bc48-44b9-abf3-68024654aed92024-05-06WarningsExact identifier
spl set id: be7fc3d4-bc48-44b9-abf3-68024654aed9

Reported adverse events (FAERS/openFDA)#

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