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Eha Lotion

Generic name: lidocaine hydrochloride
Dosage form: lotion
Drug class: Topical anesthetics

Medically reviewed by Drugs.com. Last updated on Oct 22, 2021.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Facts

Active Ingredients

Lidocaine HCI 4%

Purpose

External Anesthetic

Uses

For temporary relief of pain and itching and minor skin irritations due to minor cuts and scrapes, sunburns, and minor burns.

Warning

For external use only.

Avoid contact with eyes

Stop using this product and ask doctor if

  • symptoms last for more than seven days, or clear up and occur again within a few days
  • if redness, irritation, swelling, pain or other symptoms increase

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

For adults and children two-years or older, apply externally to the affected area. Do not use more than three to four times per day.

Inactive ingredients

Inactive ingredients: Aqua (Deionized Water), C13-14 Isoparaffin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Seed Oil, Isopropyl Myristate, Laureth-7, M Polyacrylamide, Steric Acid.

Principal Display Panel - 88 mL Bottle Label

‘Eha Lotion 4%

Pain Relief Lotion

For Professional Use Only

3 OZ (88 mL)

Distributed by

Enovachem

PHARMACEUTICALS

Torrance, CA 90501

(310) 320-0100

EHA
lidocaine hydrochloride lotion
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:76420-351
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE ANHYDROUS 4 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
C13-14 ISOPARAFFIN
GLYCERYL MONOSTEARATE
HELIANTHUS ANNUUS FLOWERING TOP
ISOPROPYL MYRISTATE
LAURETH-7
METHYLISOTHIAZOLINONE
STEARIC ACID
Packaging
# Item Code Package Description
1 NDC:76420-351-30 88 mL in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 06/07/2016
Labeler - Asclemed USA, Inc. (059888437)
Asclemed USA, Inc.