Base Numb Spray - Topical Anesthetic Spray

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, menthol spray 
Joonem LLC

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Base Numb Spray - Topical Anesthetic Spray

Drug Facts

Active ingredients

Lidocaine 4%

Menthol 1%

Purpose

Topical Analgesic

Indications:

Temporary relieves minor pain

Warnings:

Avoid contact with the eyes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician

• Do not apply to wounds or damaged skin.
• Do not bandage tightly. 
• Do not use in large quantities, particularly over raw surfaces or blistered areas.

Keep out of reach of children to avoid accidental ingestion!

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

Directions:

• use only as directed
• adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
• Children under 12 years of age: consult a doctor

Other Information:

Store at 20 to  25 C (68 to 77 F)

Inactive Ingredients:

L-arginine, Sodium Benzoate, Rectified Spirit, Disodium EDTA, Phenoxyethanol, Polysorbate 20, DM Water

Package Labeling:

BASE NUMB TOPICAL ANESTHETIC 
lidocaine, menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80327-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ARGININE (UNII: 94ZLA3W45F)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80327-003-01	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020	03/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	09/01/2020	03/31/2022

Labeler - Joonem LLC (117633878)

Revised: 1/2024

Document Id: 0df94727-7e1b-1dd6-e063-6394a90ad394

34390-5

Set id: af743be4-4054-0e74-e053-2a95a90a979d

Version: 3

Effective Time: 20240102

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