MAXOCAINE Topical Anesthetic Cream

Manufacturer
Prime Commerce, LLC
Effective date
2019-07-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:17:36

Label at a glance#

ProductMAXOCAINE Topical Anesthetic
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure6 sections

Dosage and administration

When practical, cleanse the affected area with mild soap and warm water, then rinse thoroughly. Gently dry by patting or blotting with toilet tissue or soft cloth before application of this product. Adults and children 12-years and over: apply externally to the affected area up to five times per day. Children under 12 years: Consult a physician.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 5.0%

OTC - PURPOSE SECTION

Topical Analgesic

Use:

INDICATIONS & USAGE SECTION

Relieves pain and discomfort associated with hemorrhoids and other anorectal disorders.

Warnings:

WARNINGS SECTION

For external use only

  • Avoid contact with eyes.

Do not

OTC - DO NOT USE SECTION

exceed recommended daily dosage unless directed by physician.

Stop use and consult physician

OTC - STOP USE SECTION

if rectal bleeding occurs, if allergic reaction develops, if condition worsens or does not improve within seven days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, consult physician.

Directions:

DOSAGE & ADMINISTRATION SECTION

When practical, cleanse the affected area with mild soap and warm water, then rinse thoroughly. Gently dry by patting or blotting with toilet tissue or soft cloth before application of this product.

  • Adults and children 12-years and over: apply externally to the affected area up to five times per day.
  • Children under 12 years: Consult a physician.

Other Ingredients:

INACTIVE INGREDIENT SECTION

Acrylates C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Extract, Boswellia Serrata Extract, Cannabis Sativa (Full Spectrum Hemp) Oil, Cetyl Alcohol, Dimethicone, Ethylhexylglycerin, Ilex Paraguariensis (Yerba Mate’) Extract, Isopropyl Myristate, Methylsulfonylmethane (MSM), Phenoxyethanol, Polysorbate-20, Stearic Acid, Triethanolamine.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72188-06672188-066-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d58df976-b78a-cd8a-e053-2a95a90a8cf634b6a778-88e7-44ce-98a0-c8a23b8841352022-01-14WarningsExact identifier
spl set id: 34b6a778-88e7-44ce-98a0-c8a23b884135

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.