ELECTRUM NUMB ANESTHETIC- lidocaine hcl spray

ELECTRUM NUMB ANESTHETIC by

Drug Labeling and Warnings

ELECTRUM NUMB ANESTHETIC by is a Otc medication manufactured, distributed, or labeled by RENU LABORATORIES, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Lidocaine HCl 4%

PURPOSE

Purpose

Topical Anesthetic

INDICATIONS & USAGE

Uses

For the temporary relief of pain associated with minor skin procedures

WARNINGS

Warnings

For external use only

DO NOT USE

Do Not Use

• on large areas of the body or on cut, irritated or swollen skin
• on puncture wounds
• for more than one week without consulting a doctor

WHEN USING

When using this product

• Use only as directed. Read and follow all directions and warnings on this label.
• rare cases of serious burns have been reported with products of this type
• do not bandage or apply local heat (such as heating pads) to the area of use or use with a medicated patch
• avoid contact with eyes and mucous membranes
• a transient burning sensation may occur upon applicator but generally disappears in several days

STOP USE

Stop use and ask a doctor if

• Condition worsens
• redness is present
• irritation develops
• symptoms persist for more than 7 days or clear up and occur again within a few days
• you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children and pets

• If swallowed, get medical help or contact a poison control center right away

DOSAGE & ADMINISTRATION

Directions

adults and children over 12 years:

• apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period
• after applying, wash hands with soap and water
• children 12 years or younger - ask a doctor

INACTIVE INGREDIENT

Inactive Ingredients: Aloe Barbadensis Leaf Powder, Benzyl Alcohol, Deionized Water, Disodium EDTA, Ethyl Alcohol SD 40B, Glycerin

STORAGE AND HANDLING

Other Information:

Store at 20-25° C (68 - 77°F)

QUESTIONS

Questions?

574-975-3632

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ELECTRUM NUMB ANESTHETIC 
lidocaine hcl spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76348-600
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	4.48 g  in 112 g

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZYL ALCOHOL (UNII: LKG8494WBH)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76348-600-04	112 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	11/23/2020

Labeler - RENU LABORATORIES, INC. (945739449)

Establishment
Name	Address	ID/FEI	Business Operations
RENU LABORATORIES, INC.		945739449	manufacture(76348-600)