Nupharmisto Tattoo Numbing Cream

Manufacturer
Ehy Holdings LLC
Effective date
2023-02-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:54:07

Label at a glance#

ProductNupharmisto Tattoo Numbing Cream
Active ingredientLIDOCAINE
Label structure14 sections

Dosage and administration

Adults: When practical, cleanse the affected area with mild soap and warm water and rise thoroughly. Gently dry by patting with toilet tissue or a soft cloth, before application of this product. Apply up to 6 times a day. Children under 12 years of age: consult a doctor

Storage and handling

Keep away from direct sunlight or heat. Store at room tempetature 15°-30°C (59°-86°F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 5%

Purpose

OTC - PURPOSE SECTION

Local Anesthetic

Use

INDICATIONS & USAGE SECTION

For the temporary relief of local and anorectal discomfort associated with anorectal disorder or inflammation.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Pregnant or breastfeeding, ask a health professional before use.
In case of accidental overdose, get medical help or contact the
Poison Control Center immediately.
Seal is broken or missing

OTC - WHEN USING SECTION

directed by a doctor.
certain persons can develop allergic reactions to ingredients
in this product.
do not put this product into the rectum by using finger or
any medical device or applicator

OTC - STOP USE SECTION

the symptom being treated does not subside, or if redness

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Adults: When practical, cleanse the affected area with mild soap
and warm water and rise thoroughly.
Gently dry by patting with toilet tissue or a soft cloth, before
application of this product.
Apply up to 6 times a day.
Children under 12 years of age: consult a doctor

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: When practical, cleanse the affected area with mild soap
and warm water and rise thoroughly.
Gently dry by patting with toilet tissue or a soft cloth, before
application of this product.
Apply up to 6 times a day.
Children under 12 years of age: consult a doctor

Other information

STORAGE AND HANDLING SECTION

Keep away from direct sunlight or heat.
Store at room tempetature 15°-30°C (59°-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

OTC - ASK DOCTOR SECTION

irritation, swelling, pain, or other symptoms develop or increase

OTC - QUESTIONS SECTION

service@nupharco.com

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

81799-008-01 1

81799-008-01 181799-008-01 1

81799-008-01 2

81799-008-01 281799-008-01 2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81799-008-012024-07-30C16284748780-11030e365-282d-111a-e063-dadaa90a10e281799-008 Nupharmisto Tattoo Numbing Cream
81799-008-012024-01-30C16284748780-11030e365-282d-111a-e063-dadaa90a10e281799-008 Nupharmisto Tattoo Numbing Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81799-008-01Nupharmisto Tattoo Numbing Cream50 mL in 1 BOTTLECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81799-008NUPHARMISTO TATTOO NUMBING CREAM (TATTOO NUMBING CREAM) CREAM [EHY HOLDINGS LLC]11 package rows20230216_f4be3cb8-7015-1b65-e053-2995a90a3955.zip

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
81799-00881799-008-01

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
f4be3cb8-7017-1b65-e053-2995a90a3955f4be3cb8-7015-1b65-e053-2995a90a39552023-02-15WarningsExact identifier
spl id: f4be3cb8-7017-1b65-e053-2995a90a3955
spl set id: f4be3cb8-7015-1b65-e053-2995a90a3955

Reported adverse events (FAERS/openFDA)#

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