Base Laboratories Base Numb Extra Strength Topical Anorectal Cream

Manufacturer
Joonem LLC
Effective date
2020-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:04:39

Label at a glance#

ProductBase Laboratories Base Numb Extra Strength Topical Anorectal
Active ingredientLIDOCAINE
Label structure7 sections

Dosage and administration

Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly or by patting or blotting with an appropriate cleansing pad. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Apply externally to the affected area up to 6 timess daily.  Children under 12 years of age: consult a doctor.  

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 5%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Indications

INDICATIONS & USAGE SECTION

For the temporary relief of pain and discomfort associated with anorectal disorder

Warnings

WARNINGS SECTION

If condition worsens or does not improve within 7 days, consult a doctor.

  • Do not exceed the recommended daily dosage unless directed by a doctor.
  • In case of bleeding, consult a doctor promptly.
  • Do not put this product into the rectum by using fingers or any mechanical device or applicator.
  • Certain persons can develop allergic reactions to ingredients in this product. If symptoms being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increases, discontinue use and consult a doctor.

Keep out of reach of children to avoid accidental ingestion!

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly or by patting or blotting with an appropriate cleansing pad. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Apply externally to the affected area up to 6 timess daily. 
  • Children under 12 years of age:
  • consult a doctor.  

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera, Chamomile, Tea Trea Oil, Clove Oil, Hemp Seed Oil, Zinc Oxide, Glycerin, Stearic Acid, EDTA, Arlacel 165, Carbopol U-10, Cetyl Alcohol, BHT, Cetearyl Alcohol, Cetearyl Glucoside, Phenoxyethanol, Ethylhexylglycerin, Menthol, Cyclopentasiloxane, Phenyl Trimethicone, Dimethicone, C12-15 Alkyl Benzoate, Dimethicone Crosspolymer, Caustic Soda/Sodium Hydroxide, Capric Caprylic Triglyceide, DM Water

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80327-00480327-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
0df98075-28f5-86ac-e063-6394a90a5d42b57daec8-368c-6b59-e053-2a95a90a45102024-01-02WarningsExact identifier
spl set id: b57daec8-368c-6b59-e053-2a95a90a4510

Reported adverse events (FAERS/openFDA)#

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