SCALP TECH - THE SOLUTION (82617-110)

Manufacturer
SCALP TECH INC
Effective date
2026-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-12 01:00:54

Label at a glance#

ProductTHE SOLU TION
Active ingredientLIDOCAINE HYDROCHLORIDE, EPINEPHRINE HYDROCHLORIDE
Label structure13 sections

Indications and uses

FOR THE TEMPORARY RELIEF OF LOCAL AND ANORECTAL ITCHING, DISCOMFORT, AND PAIN ASSOCIATED WITH ANORECTAL DISORDERS OR ANORECTAL INFLAMMATION.

Dosage and administration

ADULTS AND CHILDREN UNDER 12 YEARS OF AGE, CONSULT A DOCTOR. CLEAN THE AFFECTED AREA WITH MILD SOAP AND WATER. RINSE WELL OR PAT WITH APROPRIATE CLEANSING PAD GENTLY DRY BY PATTING OR BLOTTING WITH TOILET TISSUE OR A SOFT CLOTH BEFORE APPLYING THIS PRODUCT USE SPRAY PUMP TO APPLY EXTERNALLY TO THE AFFECTED AREA UP TO 4 TIMES DAILY DO NOT USE MORE OFTEN THAN DIRECTED

Storage and handling

STORE AT ROOM TEMPERATURE (15-30C)

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

LIDOCAINE HCL 5%

EPINEPHRINE HCL .01%

PURPOSE

OTC - PURPOSE SECTION

LOCAL ANESTHETICS

VASOCONSTRICTOR

USES

INDICATIONS & USAGE SECTION

FOR THE TEMPORARY RELIEF OF LOCAL AND ANORECTAL ITCHING, DISCOMFORT, AND PAIN ASSOCIATED WITH ANORECTAL DISORDERS OR ANORECTAL INFLAMMATION.

WARNINGS

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY.
  • AVOID CONTACT WITH THE EYES.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IF SWALLOWED, CALL A POISON CONTROL CENTER OR GET MEDICAL HELP RIGHT AWAY.

DO NOT USE THIS PRODUCT IF:

OTC - DO NOT USE SECTION

  • YOU HAVE A HEART CONDITION, HIGH BLOOD PRESSURE, THYROID DISEASE, DIABETES, OR DIFFICULTY IN URINATION DUE TO ENLARGEMENT OF PROSTATE GLAND UNLESS DIRECTED BY A DOCTOR.

WHEN USING THIS PRODUCT:

OTC - WHEN USING SECTION

  • DO NOT PUT THIS PRODUCT INTO THE RECTUM BY USING FINGERS OR ANY MEDICAL DEVICE OR APPLICATOR.

STOP USE AND ASK A DOCTOR IF:

OTC - STOP USE SECTION

  • IF BLEEDING OCCURS, CONDITION WORSENS OR DOES NOT IMPROVE WITHIN 7 DAYS
  • REDNESS, IRRITATION, SWELLING, PAIN OR ANY OTHER SYMPTOMS OCCUR
  • YOU EPERIENCE WEAKNESS, CONFUSION, HEADACHE, DIFFICULTY BREATHING
  • PALE, GREY OR BLUE COLOURED SKIN
  • THESE MAY BE SIGN OF METHEMOGLOBINEMIA, A RARE DISORDER, WHICH MAY APPEAR UP TO 2 HOURS AFTER USE

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • ADULTS AND CHILDREN UNDER 12 YEARS OF AGE, CONSULT A DOCTOR.
  • CLEAN THE AFFECTED AREA WITH MILD SOAP AND WATER.
  • RINSE WELL OR PAT WITH APROPRIATE CLEANSING PAD
  • GENTLY DRY BY PATTING OR BLOTTING WITH TOILET TISSUE OR A SOFT CLOTH BEFORE APPLYING THIS PRODUCT
  • USE SPRAY PUMP TO APPLY EXTERNALLY TO THE AFFECTED AREA UP TO 4 TIMES DAILY
  • DO NOT USE MORE OFTEN THAN DIRECTED

OTHER INFORMATION

STORAGE AND HANDLING SECTION

  • STORE AT ROOM TEMPERATURE (15-30C)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, ETHOXYDIGLYCOL, PHENOXETHANOL, ALLANTOIN, ETHYHEXYGLYCERIN

QUESTIONS?

OTC - QUESTIONS SECTION

+ 1 (403) 901-8244

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
82617-11082617-110-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
THE SOLU TIONLIDOCAINE HYDROCHLORIDE AND EPINEPHRINE HYDROCHLORIDESCALP TECH INC58793581-8826-9a74-e063-6294a90a24652026-08-06WarningsExact identifier
ndc (package): 82617-110-01
ndc (product): 82617-110
ndc11 (package): 82617011001
spl id: 5879358d-b3e8-9791-e063-6294a90ad014
spl set id: 58793581-8826-9a74-e063-6294a90a2465

Reported adverse events (FAERS/openFDA)#

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