Skip to Content

Procicept B Benzocaine 20%

Medically reviewed on January 20, 2018

Dosage form: liquid
Ingredients: BENZOCAINE 0.2g in 1g, MENTHOL 0.01g in 1g
Labeler: Nocicept Technologies, Inc.
NDC Code: 70458-102

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.

Drug Facts

Active Ingredients                              Purpose

Benzocaine  20%                                   Topical Anesthetic

Menthol 1%                                           Topical Analgesic

Uses

Temporarily relieves minor pain.

Warnings

For external use only

Do not use
On large areas of the body or on cut, irritated or swollen skin
On puncture wounds
For more than one week without consulting a doctor

When using this product

Use only as directed

Read and follow all direction and warnings on this carton

Do not allow contact with eyes

Do not bandage or apply local heat (such as heating pads) to the area of use

Stop using and ask a doctor if

Condition worsens

Symptoms persist for more than 7 days or clear up and occur again within a few days

When pregnant or breastfeeding, ask a health professional before use

Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Adults and children over 12 years of age

Apply generously (about the thickness of a nickel) to the affected area as needed, not to exceed 3 applications

Children 12 years and younger

Ask a doctor

Inactive ingredients

benzyl alcohol, soy lecithin, isopropyl palmitate, poloxamer, sorbic acid

PROCICEPT B  BENZOCAINE 20%
benzocaine and menthol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70458-102
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (BENZOCAINE) BENZOCAINE0.2 g  in 1 g
MENTHOL (MENTHOL) MENTHOL0.01 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL 
LECITHIN, SOYBEAN 
ISOPROPYL PALMITATE 
POLOXAMER 124 
SORBIC ACID 
Packaging
#Item CodePackage Description
1NDC:70458-102-021 TUBE, WITH APPLICATOR in 1 CARTON
15 g in 1 TUBE, WITH APPLICATOR
2NDC:70458-102-20200 g in 1 JAR
3NDC:70458-102-071 TUBE in 1 CARTON
37.5 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/01/201712/31/2019
Labeler - Nocicept Technologies, Inc. (080111681)

 
Nocicept Technologies, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide