ELECTRUM NUMB FOAM- lidocaine hci soap

Electrum Numb Foam by

Drug Labeling and Warnings

Electrum Numb Foam by is a Otc medication manufactured, distributed, or labeled by RENU LABORATORIES, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

For external use only

• avoid contact with eyes
• do not exceed recommended dosage unless directed by a doctor

Do not use

• in the eyes or apply to large areas of body
• longer than 1 week unless directed by a doctor
• in large quantities particularly over raw surfaces or blistered areas
• ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns

STOP USE

Stop Use and ask a doctor if

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

INACTIVE INGREDIENT

Inactive Ingredients: Allantoin, Aloe Barbadensis (Aloe) Powder, Arnica Montana (Arnica) Extract, Caprylyl Glycol, Cocoamidopropyl Betaine, Deionized Water, Disdoium Cocoamphodiacetate, Glycerin, Hexylene Glycol, Phenoxyethanol, Sodium Chloride.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:

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

QUESTIONS

Questions? 574-975-3632

ACTIVE INGREDIENT

Active Ingredient

Lidocaine HCL 4%

PURPOSE

Purpose

Topical anesthetic

First aid antiseptic

STATEMENT OF IDENTITY

ELECTRUM NUMB FOAM FOAMING ANESTHETIC

DOSAGE & ADMINISTRATION

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ELECTRUM NUMB FOAM 
lidocaine hci soap

Product 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)