Label: DR. NUMB- lidocaine and benzethonium chloride cream cream
- NDC Code(s): 69903-002-50
- Packager: Shinpharma Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 3, 2024
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- Active Ingredient
- Purpose
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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.
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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
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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
- Inactive Ingredients
- Question or comments?
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INGREDIENTS AND APPEARANCE
DR. NUMB
lidocaine and benzethonium chloride cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69903-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 mg in 50 g BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.25 mg in 50 g Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) BENZYL ALCOHOL (UNII: LKG8494WBH) GLYCERIN (UNII: PDC6A3C0OX) LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) 3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH) PHENOXYETHANOL (UNII: HIE492ZZ3T) SELAGINELLA LEPIDOPHYLLA (UNII: 02JQ564P1G) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69903-002-50 1 in 1 CARTRIDGE 09/12/2017 1 50 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 09/12/2017 Labeler - Shinpharma Inc (248552403) Registrant - Shinpharma Inc (248552403)
