DCH Numbing Relief

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LIDOCAINE 5%
DCH Numbing Relief

DCH Numbing Relief LIDOCAINE 5% DERMA CARE RESEARCH LABS, LLC FDA Approved For the local itching and pain associated with anorectal disorders or inflammation.

Generic: LIDOCAINE 5%

Mfr: DERMA CARE RESEARCH LABS, LLC FDA OTC

Substance Lidocaine

Route

TOPICAL

Applications

M015

Product NDC

72839-0173-00 72839-0173-05

Package NDC

72839-173-05

Drug Facts

Composition & Profile

Active Ingredients

Lidocaine 5%

Inactive Ingredients

Water alcohol denat. propylene glycol glycerin aloe barbadensis leaf extract tocopheryl acetate chamomilla recutita (matricaria) flower extract cucumis sativus (cucumber) fruit extract disodium cocoamphodipropionate carbomer disodium EDTA triethanolamine.

Strengths

5 %

Treats Conditions

For The Local Itching And Pain Associated With Anorectal Disorders Or Inflammation

Identifiers & Packaging

Container Type UNKNOWN

NDC 72839-0173-00

All Product Codes

72839-0173-00 72839-0173-05

UPC

0850009221834

UNII

98PI200987

SPL Set IDs

ffd70a31-7d0c-d2d0-e053-6394a90a8674

Packaging

Label

Package Descriptions

Label

Overview

For the local itching and pain associated with anorectal disorders or inflammation.

Indications & Usage

For the local itching and pain associated with anorectal disorders or inflammation.

Dosage & Administration

When practical, cleanse the affected area with mild soap and warm water, Rinse thoroughly and gently pat dry. Spray affected area. Wash hands after applying. Adults and children 2 years of age and older, apply externally to the affected area up to 6 times a day. Children under 12 years of age: consult a doctor.

Warnings & Precautions

For external use only. Flammable-- Keep away from fire or flame. When using this product avoid contact with eyes, do not exceed recommended dosage unless directed by a doctor, do not put this product into the rectum by using fingers or any mechanical device or applicator, contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120F. Stop use and ask a doctor if rectal bleeding occurs, condition worsens or does not improve within 7 days, allergic reaction occurs to ingredients in this product, symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase. i

Purpose

Topical anesthetic

Keep Out of Reach of Children

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