BASE LABORATORIES LIDOCAINE ANESTHETIC PAIN RELIEF- lidocaine cream

Base Laboratories Lidocaine Anesthetic Pain Relief by

Drug Labeling and Warnings

Base Laboratories Lidocaine Anesthetic Pain Relief by is a Otc medication manufactured, distributed, or labeled by Joonem LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Lidocaine 4%

Purpose

Topical Analgesic

Indications:

Temporary relieves minor pain

Warnings:

For external use only

• 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 25 C (68 to 77 F)

Inactive Ingredients:

Hemp Seed Oil, Aloe Vera Extract, Chamomile Extract, Glycerol, Cetearyl Alcohol, Cetearyl Glucoside, Propylene Glycol, Laurocapram, Stearic Acid, Glyceryl Stearate, PEG-100, EDTA, Cetyl Alcohol, Triethanolamine, Water

Package Labeling:

INGREDIENTS AND APPEARANCE

BASE LABORATORIES LIDOCAINE ANESTHETIC PAIN RELIEF 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80327-010
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

Inactive Ingredients
Ingredient Name	Strength
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CHAMOMILE (UNII: FGL3685T2X)
GLYCERIN (UNII: PDC6A3C0OX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
LAUROCAPRAM (UNII: 1F3X9DRV9X)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
POLYETHYLENE GLYCOL 4500 (UNII: TVH7653921)
EDETIC ACID (UNII: 9G34HU7RV0)
CETYL ALCOHOL (UNII: 936JST6JCN)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80327-010-60	1 in 1 CARTON	08/31/2022
1		60 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/31/2022

Labeler - Joonem LLC (117633878)