Label: ELECTRUM NUMB FOAM- lidocaine hci soap
- NDC Code(s): 76348-596-17
- Packager: RENU LABORATORIES, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 20, 2024
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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, tattoo, dermarolling, electrolysis, microblading and piercing.
- Temporarily relieves pain and itch while helping prevent infection
Directions
- Shake Well before each use. Apply 2 to 3 pumps of foam soap and gently rub into skin. Leave it on for 5 to 10 minutes. Rinse off gently with running water or wipe with a clean paper towel. Use before, during and after the procedure. Keep bottle tightened to keep product fresh and effective. Adults and children 2 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 3 times a day.
- Children under two years of age, ask a doctor
- WARNINGS
- STOP USE
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- QUESTIONS
- ACTIVE INGREDIENT
- PURPOSE
- STATEMENT OF IDENTITY
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ELECTRUM NUMB FOAM
lidocaine hci soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76348-596 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 1.92 g in 48 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) PHENOXYETHANOL (UNII: HIE492ZZ3T) ARNICA MONTANA (UNII: O80TY208ZW) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) GLYCERIN (UNII: PDC6A3C0OX) BENZETHONIUM CHLORIDE (UNII: PH41D05744) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76348-596-17 48 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/29/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 07/29/2021 Labeler - RENU LABORATORIES, INC. (945739449) Establishment Name Address ID/FEI Business Operations RENU LABORATORIES, INC. 945739449 manufacture(76348-596)