Mirakel Pain Relief Roll-On LIDOCAINE HCL SANVIO, INC. FDA Approved Temporarily relieves minor pain.
FunFoxMeds box
Route
TOPICAL
Applications
M017
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
Lidocaine HCl 4%
Inactive Ingredients
Water Alcohol Denat. Glyceryl Stearate Cetearyl Alcohol Dimethicone Aminomethyl Propanol Aloe Barbadensis Leaf Extract Arnica Montana Flower Extract Salix Alba (Willow) Bark Extract Curcuma Longa (Turmeric) Root Extract Mentha Piperita (Peppermint) Leaf Extract Eucalyptus Globulus Leaf Oil Glycerin Acrylates/C10-30 Alkyl Acrylate Crosspolymer C30-45 Alkyl Cetearyl Dimethicone Crosspolymer Caprylyl Methicone Ceteth-20 Phosphate Dicetyl Phosphate Disodium EDTA Ethylhexylglycerin Steareth-21 Methylparaben
Strengths
4 %
Treats Conditions
Temporarily Relieves Minor Pain

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UPC
0860008420022
UNII
V13007Z41A
Packaging

Label

Package Descriptions
  • Label

Overview

Temporarily relieves minor pain.

Indications & Usage

Temporarily relieves minor pain.

Dosage & Administration

Clean affected area before applying product. Adults and children 12 years and older : apply to the affected area not more than 3 to 4 times daily. Children under 12 years old: ask a doctor.

Warnings & Precautions
For external use only. Flammable-- keep away from fire or flame. Do not use if you have an allergic reaction to lidocaine or other local anesthetics on large areas of the body or on cut, irritated, blistered, or swollen skin on puncture wounds for more than one week without consulting a doctor Stop use and ask a doctor if condition worsens severe burning sensation, redness, rash, or irritation develops symptoms persist for more than 7 days or clear p and occur again within a few days you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied
Purpose

Topical anesthetic

Keep Out of Reach of Children

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


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