Aspercreme Lidocaine Foot (Diabetic) LIDOCAINE HYDROCHLORIDE CHATTEM, INC. FDA Approved Use temporarily relieves minor pain
FunFoxMeds box
Route
TOPICAL
Applications
M017
Product NDC
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
Active ingredient Lidocaine HCl 4%
Inactive Ingredients
Inactive ingredients water alcohol denat. (10%) cetearyl alcohol ceteth-20 phosphate dimethicone caprylyl methicone dicetyl phosphate glyceryl stearate aloe barbadensis leaf juice panthenol tocopheryl acetate magnesium ascorbyl phosphate aminomethyl propanol C30-45 alkyl cetearyl dimethicone crosspolymer acrylates/C10-30 alkyl acrylate crosspolymer ethylhexylglycerin methylparaben disodium EDTA citric acid 333-105 Child-resistant packaging. Close cap tightly after use.
Strengths
4 %
Quantities
2 count
Treats Conditions
Use Temporarily Relieves Minor Pain

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UNII
V13007Z41A
Packaging

PRINCIPAL DISPLAY PANEL Max Strength Aspercreme Lidocaine 2 in 1 Pain Relief + Moisturization foot cream PRINCIPAL DISPLAY PANEL Max Strength Aspercreme Lidocaine 2 in 1 Pain Relief + Moisturization foot cream

Package Descriptions
  • PRINCIPAL DISPLAY PANEL Max Strength Aspercreme Lidocaine 2 in 1 Pain Relief + Moisturization foot cream PRINCIPAL DISPLAY PANEL Max Strength Aspercreme Lidocaine 2 in 1 Pain Relief + Moisturization foot cream

Overview

Use temporarily relieves minor pain

Indications & Usage

Use temporarily relieves minor pain

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 ■ massage into painful area until thoroughly absorbed into skin children 12 years or younger : ask a doctor

Warnings & Precautions
Warnings For external use only Do not use ■ if you have serious foot problems, such as ulcers or infections ■ if you have numbness or reduced ability to feel pain ■ on cut, irritated or swollen skin ■on puncture wounds ■ for more than one week without consulting a doctor When using this product ■ use only as directed. Read and follow all directions and warning on this carton. ■ do not allow contact with the eyes and the mucous membranes ■ do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use ■ do not use at the same time as other topical analgesics 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 If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Purpose

Purpose Topical anesthetic

Do Not Use

Do not use ■ if you have serious foot problems, such as ulcers or infections ■ if you have numbness or reduced ability to feel pain ■ 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 warning on this carton. ■ do not allow contact with the eyes and the mucous membranes ■ do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use ■ do not use at the same time as other topical analgesics

Stop Use & Ask a Doctor

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

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.


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