Relieve A Pain LIDOCAINE RELIEVE A PAIN LLC FDA Approved Uses For temporary relief of pain and itching.

RELIEVE A PAIN

Generic: LIDOCAINE
Mfr: RELIEVE A PAIN LLC FDA OTC
FunFoxMeds box
Substance Lidocaine
Route
TOPICAL
Applications
M017
Product NDC
87198-0001-00 87198-0001-01
Package NDC
87198-001-01

Drug Facts

Composition & Profile

Active Ingredients
Active Ingredients Lidocaine HCL 4.0% w/w
Inactive Ingredients
Inactive Ingredients Arnica Montana Flower Extract C13-14 Isoparaffin Chondroitin Sulfate Dimethyl Sulfone (MSM) Emu Oil Ethylhexylglycerin Glucosamine Sulfate Glycerin Isopropyl Palmitate Laureth-7 Phenoxyethanol Polyacrylamide Propylene Glycol Stearic Acid Triethanolamine Water
Strengths
4.0 %
Treats Conditions
Uses For Temporary Relief Of Pain And Itching

Identifiers & Packaging

Container Type UNKNOWN
NDC 87198-0001-00
All Product Codes
87198-0001-00 87198-0001-01
UNII
98PI200987
SPL Set IDs
cafaa830-d894-4590-8928-d579cc791d79
Packaging

Product label image description image description

Package Descriptions
  • Product label image description image description
Overview

Uses For temporary relief of pain and itching.

Indications & Usage

Uses For temporary relief of pain and itching.

Dosage & Administration

Directions For adults and children 12 years or older: Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: consult a physician.

Warnings & Precautions
Warnings For external use only Avoid contact with eyes Do not use in large quantities, particularly over raw surfaces or blistered areas. Discontinue use and consult a doctor if • Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Keep out of reach of children • If the product is swallowed, get medical help or contact a Poison Control Center right away.
Purpose

Purpose Topical Analgesic

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Additional Information

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