YOUCOPIA TATTOO NUMBING

Manufacturer
Good Manager Holdings Inc
Effective date
2023-09-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:26:32

Label at a glance#

ProductYOUCOPIA TATTOO NUMBING
Active ingredientLIDOCAINE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 5%

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center right away.

OTC - PURPOSE SECTION

Local Anesthetic

INDICATIONS & USAGE SECTION

Uses:
For the temporary relief of pain, burning, and soreness.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS:
Children under 12: Consult a doctor.
Adults and children 12 years and older: For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a clean, soft cloth before application of this product. Apply externally up to 6 times per day.

OTC - WHEN USING SECTION

WHEN USING THIS PRODUCT
do not exceed the recommended daily dosage unless directed by a doctor - do not put into the rectum by using fingers or any mechanical device or applicator

OTC - STOP USE SECTION

STOP USE AND ASK A DOCTOR IF
allergic reaction occurs
rectal bleeding occurs
redness, irritattion, swelling, pain or other symptoms begin or increase
condition worsens or does not improve within 7 days

WARNINGS SECTION

WARNINGS (For external use only)

OTHER SAFETY INFORMATION

OTHER INFORMATION
keep away from direct sunlight or heat. store in room temperature (59-86°F / 15-30°C).

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS
Carbomer 934, Emu Oil, Arnica, Lecithin(Soybean), Propylene - Glycol, Tocopheryl Acetate, Benzyl Alcohol, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABELPACKAGE LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82372-007-012025-02-12C16284748780-12cef2736-77c9-d83d-e063-dadaa90ab31f047e5246-d206-356a-e063-6394a90a5070
82372-007-012025-01-30C16284748780-12cef2736-77c9-d83d-e063-dadaa90ab31f047e5246-d206-356a-e063-6394a90a5070

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82372-00782372-007-01

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
2deaa722-e6a4-40c8-e063-6394a90a1f75047e5246-d206-356a-e063-6394a90a50702025-02-11WarningsExact identifier
spl set id: 047e5246-d206-356a-e063-6394a90a5070

Reported adverse events (FAERS/openFDA)#

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