FDA.reportPublic FDA data

Base Numb Gel Topical Anesthetic Gel

Manufacturer
Joonem LLC
Effective date
2021-04-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:47:55

Label at a glance#

ProductBase Numb Topical Anesthetic
Active ingredientLIDOCAINE
Label structure6 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 times 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 disorders

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 the symptom 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 times daily. 
  • Children under 12 years of age:
  • consult a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera, Chamomile, Tea Trea Oil, Hemp Seed Extract, Glycerin, Sodium Benzoate,TEA, Carbopol U 20, DS EDTA,DM Water

Package Label:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80327-006-012024-01-02C16284748780-1e4f33bdf-a09b-d8a0-e053-dadaa90a6e4eBase Numb Gel Topical Anesthetic Gel
80327-006-012022-07-29C16284748780-1e4f33bdf-a09b-d8a0-e053-dadaa90a6e4eBase Numb Gel Topical Anesthetic Gel

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80327-00680327-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CHAMOMILEFGL3685T2XIACT
TEA TREE OILVIF565UC2GIACT
CANNABIS SATIVA SEEDQE567Z26NGIACT
GLYCERINPDC6A3C0OXIACT
SODIUM BENZOATEOJ245FE5EUIACT
TEA LEAFGH42T47V24IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
EDETIC ACID9G34HU7RV0IACT
WATER059QF0KO0RIACT
LIDOCAINE98PI200987ACTIB

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
0dfa5830-6613-c4e5-e063-6294a90aa6a8bf010a6b-a82d-54fc-e053-2995a90aa2e42024-01-02WarningsExact identifier
spl set id: bf010a6b-a82d-54fc-e053-2995a90aa2e4

Reported adverse events (FAERS/openFDA)#

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