Base Numb Gel Topical Anesthetic Gel

Base Numb Topical Anesthetic by

Drug Labeling and Warnings

Base Numb Topical Anesthetic by is a Otc medication manufactured, distributed, or labeled by Joonem LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BASE NUMB TOPICAL ANESTHETIC- lidocaine gel 
Joonem LLC

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Base Numb Gel Topical Anesthetic Gel

Drug Facts

Active ingredients

Lidocaine 5%

Purpose

Topical Analgesic

Indications:

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

Warnings:

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!

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

Directions

• 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

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

Package Label:

BASE NUMB TOPICAL ANESTHETIC 
lidocaine gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80327-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)	Â
CHAMOMILE (UNII: FGL3685T2X)	Â
TEA TREE OIL (UNII: VIF565UC2G)	Â
CANNABIS SATIVA SEED (UNII: QE567Z26NG)	Â
GLYCERIN (UNII: PDC6A3C0OX)	Â
SODIUM BENZOATE (UNII: OJ245FE5EU)	Â
TEA LEAF (UNII: GH42T47V24)	Â
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)	Â
EDETIC ACID (UNII: 9G34HU7RV0)	Â
WATER (UNII: 059QF0KO0R)	Â

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80327-006-01	120 mL in 1 JAR; Type 0: Not a Combination Product	03/01/2021	03/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	03/01/2021	03/31/2022

Labeler - Joonem LLC (117633878)

Revised: 1/2024

Document Id: 0dfa5830-6613-c4e5-e063-6294a90aa6a8

34390-5

Set id: bf010a6b-a82d-54fc-e053-2995a90aa2e4

Version: 2

Effective Time: 20240102

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