Skip to content

Checked

OTC

Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL Numbing

lidocaine · Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL Numbing is an amide local anesthetic (over-the-counter) containing lidocaine, made by Putian Licheng District Zhijiancheng Trading Co., Ltd..

Type
Over the counter
Drug class
Amide Local Anesthetic
Route
Topical
Manufacturers
1

1.First, conduct apatch test to checkfor skin suitabilityand effectiveness. 2.Thoroughly washyour hands and thetreatment area withmild soap and warmwater, then dry. 3.Apply a THICKlayer of cream tocover the entiretreatment area andits surroundings.

Drug facts

Generic name
lidocaine
Active ingredients
Lidocaine
Dosage forms
Cream
Label holder
Putian Licheng District Zhijiancheng Trading Co., Ltd.
FDA application
M015
Label updated
08/08/2026

Active ingredients

Purpose Lidocaine 5%........Topical Analgesic

Purpose

Uses For the temporary relief of localitching and discomfort associatedwith anorectal disorders.For the temporary relief of pain,burning and soreness.

Uses

1.First, conduct apatch test to checkfor skin suitabilityand effectiveness. 2.Thoroughly washyour hands and thetreatment area withmild soap and warmwater, then dry. 3.Apply a THICKlayer of cream tocover the entiretreatment area andits surroundings.

Directions

Children under 2 years: Do not use.For children under 12: Consult adoctor. For adults: Apply to affected area notmore than 6 times daily. Clean theaffected area with mild soap andwarm water, making sure to rinsethoroughly. Gently dry the area withtoilet tissue or a soft cloth beforeapplying the product.

Warnings

For external use onlyAvoid contact with the eyes

Keep out of reach of children

If swallowed, get medical help orcontact a poison control center rightaway.

Inactive ingredients

Water, Propylene Glycol,Carbomer, Glycerin,Disodium Edta,Hydroxyacetophenone,1,2-Hexanediol, MenthaArvensis Leaf Extract.Chrysanthellum IndicumExtract, PortulacaOleracea Extract,Peg-40 HydrogenatedCastor Oil

Forms and strengths

From the FDA NDC Directory · 1 product codes

Dosage formStrengthRouteNDCs
Cream5 g/100gtopical1

Side effect reports to FDA

FDA Adverse Event Reporting System (FAERS), 57,975 reports that list lidocaine, data through 07/30/2026

Anyone can report a problem to FDA, and a report does not mean the drug caused the problem. Reports can be duplicated or incomplete, and counts depend on how widely a drug is used. Do not stop or change a medicine because of this list. Talk to your doctor or pharmacist.

Most often reported reactions

  • Drug ineffective4,341
  • Off label use4,128
  • Pain3,661
  • Fatigue3,499
  • Product adhesion issue3,452
  • Nausea3,399
  • Headache3,310
  • Product quality issue3,206
  • Sinusitis2,562
  • Dyspnea2,402

To report a side effect, use FDA MedWatch.

Manufacturers and labels

1 FDA label

  • Putian Licheng District Zhijiancheng Trading Co., Ltd.Shown hereM015 · Label 08/08/2026 · NDC 87152-003Full label

Related recalls

FDA drug recalls that name this drug or its active ingredient

All drug recalls

Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL Numbing: common questions

What is Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL Numbing used for?
1.First, conduct apatch test to checkfor skin suitabilityand effectiveness. 2.Thoroughly washyour hands and thetreatment area withmild soap and warmwater, then dry. 3.Apply a THICKlayer of cream tocover the entiretreatment area andits surroundings.
Is Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL Numbing a prescription drug?
No. Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL Numbing is sold over the counter (OTC) without a prescription.
Are there other products with the same active ingredient as Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL Numbing?
Yes. Other FDA-listed products with the same active ingredients include Pain Relief Patches, Burn Relief, LIDOCAINE PAIN RELIEF Gel-Patch, Lidocaine Numbing Cream.
Who makes Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL Numbing?
Putian Licheng District Zhijiancheng Trading Co., Ltd. lists Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL Numbing with the FDA.

Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 08/08/2026 · Label text is shown as published by the manufacturer. Not medical advice