Dr. Numb Cream
FDA Label NDC 69903-002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Shinpharma Inc for the product Dr. Numb (NDC 69903-002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, ask a doctor before use if you have, stop the use and consult doctor if:, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Lidocaine 4%

benzethonium Chloride 0.25%

Purpose

External Analgesic and First Aid Antiseptic

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.

Warnings

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

Do Not Use

  • 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

  • deep or puncture wounds, animal bites or serious burns

Stop The Use And Consult Doctor If:

  • 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

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • 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

  • Store at controlled room temperature 590​-860​F (150-300C)
  • Do not expose to temperature above 1200F(490C)
  • Protect from freezing

Inactive Ingredients

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?

Call weekdays 9 AM to 6 PM PST at 1-877-786-2001 or email us at [email protected]

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

Label (002)

Label (002)

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