Base Laboratories Numb Gel

Base Laboratories Numb Gel by

Drug Labeling and Warnings

Base Laboratories Numb Gel by is a Otc medication manufactured, distributed, or labeled by JOONEM LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BASE LABORATORIES NUMB GEL- lidocaine, menthol gel 
JOONEM LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Base Laboratories Numb Gel

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 the 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 25C (68 to 77 F)

Inactive Ingredients:

Glycerol, Propylene Glycol, Alcohol, GPL, Hydroxyethyl Cellulose, Water

Package Labeling:

BASE LABORATORIES NUMB GEL 
lidocaine, menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80327-007
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
GLYCERIN (UNII: PDC6A3C0OX)	Â
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	Â
ALCOHOL (UNII: 3K9958V90M)	Â
LIQUEFIED PETROLEUM GAS (UNII: 5K616HU99V)	Â
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)	Â
WATER (UNII: 059QF0KO0R)	Â

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80327-007-01	1 in 1 CARTON	08/01/2021	11/01/2022
1		120 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/01/2021	11/01/2022

Labeler - JOONEM LLC (117633878)

Revised: 1/2023

Document Id: f1721f8f-9966-cb01-e053-2995a90aa2ff

34390-5

Set id: c939a561-4dcd-5d5e-e053-2a95a90a8451

Version: 3

Effective Time: 20230104

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