Drug Facts

Manufacturer
Shinpharma Inc
Effective date
2026-04-30
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:55:48

Label at a glance#

ProductDr. Numb
Active ingredientLIDOCAINE, BENZETHONIUM CHLORIDE
Label structure9 sections

Indications and uses

Can be used instead of soap and water to help clean minor cuts, scrapes, and burns For the temporary relief of discomfort and pain associated with dermal procedures such as tattoo removal, dermarolling, electrolysis, microblading, and piercing Temporarily relieves pain and itch while helping to prevent infection.

Dosage and administration

Use Dr.Numb® Topical Anesthetic Foam Soap to cleanse the targeted area. Shake well before each use. Apply 2 to 3 pumps of foam soap andgently rub into the skin. Leave it onfor 5 to 10 minutes. Rinse off gentlywith running water or wipe with cleanpaper towel. Use before, during andafter the procedure. Make sure tocover the bottle tightly when not inuse, otherwise, the anesthetic effect will be lessened. Adults and ...

Storage and handling

Store at controlled room temperature 59 0 ​-86 0 ​F (15 0 -30 0 C) Do not expose to temperature above 120 0 F(49 0 C) Protect from freezing

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

benzethonium Chloride 0.25%

Purpose

OTC - PURPOSE SECTION

External Analgesic and First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Can be used instead of soap and water to help clean minor cuts, scrapes, and burns
  • For the temporary relief of discomfort and pain associated with dermal procedures such as tattoo removal, dermarolling, electrolysis, microblading, and piercing
  • Temporarily relieves pain and itch while helping to prevent infection.

Warnings

WARNINGS SECTION

  • For external use only
  • avoid contact with eyes ​​

Do not use

OTC - DO NOT USE SECTION

  • do not use in large quantities particularly over raw surfaces or blistered area
  • do not exceed the recommended dosage unless directed by a doctor
  • in the eyes or apply over large areas of body
  • longer than one week unless directed by a doctor

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds, animal bites or serious burns

Stop the use and consult doctor if:

OTC - STOP USE SECTION

  • condition worsenss or symptoms persist for more than 7 days or clear up and occur again within few days.

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

  • Use Dr.Numb® Topical Anesthetic Foam Soap to cleanse the targeted area.
  • Shake well before each use.
  • Apply 2 to 3 pumps of foam soap andgently rub into the skin. Leave it onfor 5 to 10 minutes. Rinse off gentlywith running water or wipe with cleanpaper towel.
  • Use before, during andafter the procedure.
  • Make sure tocover the bottle tightly when not inuse, otherwise, the anesthetic effect will be lessened.

Adults and children two years old and older: Use to clean minor cuts, scrapes, and burns by thoroughly washing with water. Rinse and air dry. Use no more than three times daily.

Children under two years of age, ask a doctor.

Other information

STORAGE AND HANDLING SECTION

  • Store at controlled room temperature 59 0​-86 0​F (15 0-30 0C)
  • Do not expose to temperature above 120 0F(49 0C)
  • Protect from freezing

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Allantoin, Aloe Barbadensis Leaf Juice, Arnica Montana Flower Extract, Benzyl Alcohol, Glycerin , Lauramidopropyl Betaine, Leuconostoc/Radish Root Ferment Filtrate, Menthoxypropanediol, Phenoxyethanol, Selaginella Lepidophylla Extract, Sodium Hydroxide, Water.

Question or comments?

OTC - QUESTIONS SECTION

Call weekdays 9 AM to 6 PM PST at 1-877-786-2001 or email us at support@drnumb.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 69903-002-50

Dr.Numb

TOPICAL ANESTHETIC FOAM SOAP

4% LIDOCAINE

0.25% BENZETHONIUM CHLORIDE

DISINFECT DESENSITIZE and RELAX

1.7 oz

LabelLabel

DailyMed Pharmacologic Classes#

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.drnumb.com/002.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69903-002-502024-04-03C16284748780-1ba0f9c33-57b1-a910-e053-dadaa90a0b85Drug Facts
69903-002-502024-01-30C16284748780-1ba0f9c33-57b1-a910-e053-dadaa90a0b85Drug Facts
69903-002-502021-02-12C16284748780-1ba0f9c33-57b1-a910-e053-dadaa90a0b85Drug Facts
69903-002-502021-01-29C16284748780-1ba0f9c33-57b1-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69903-002-50Dr. Numb1 in 1 CARTRIDGECREAM16
69903-002-50Dr. Numb50 g in 1 TUBECREAM506

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69903-00269903-002-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Dr. NumbLIDOCAINE AND BENZETHONIUM CHLORIDE CREAMShinpharma Incd8cdccdb-775b-4970-a6ea-50b62df221d62026-04-30WarningsExact identifier
ndc (package): 69903-002-50
ndc (product): 69903-002
ndc11 (package): 69903000250
spl id: 50b50aba-23c0-623d-e063-6394a90ab2eb
spl set id: d8cdccdb-775b-4970-a6ea-50b62df221d6

Reported adverse events (FAERS/openFDA)#

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