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Bed Bug Instant Bite Relief

Medically reviewed on February 8, 2018

Dosage form: gel
Ingredients: LIDOCAINE 40mg in 1g
Labeler: P.F. Harris Mfg. Co. LLC
NDC Code: 70466-001

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.

Bed Bug Instant Bite Relief Gel

Drug Facts

Active Ingredients

Lidocaine 4%

Purpose

Topical Anesthetic

Uses:

For the temporary relief of discomfort and pain associated with • minor burns and skin irritations • minor cuts and scrapes • itching.

Directions:

Adults and children 12 years of age and older: Apply to affected area not more than 3-4 times daily.

Warnings:

For external use only. Avoid contact with the eyes.

Do not use

in large quantities, particularly over raw or blistered areas.

Stop use and ask a doctor if

•skin becomes irritated • condition worsens or sysmptoms last than 7 days • symptoms clear up and recur within a few days.

Inactive Ingredients:

Aloe Barbadensis Leaf Juice, Calendula Officinalis Flower Extract, Camellia Sinensis (Green Tea) Leaf Extract, Carbomer, Chamomilla Recutita (Matricaria) Flower Extract, Diazolidinyl Urea, Disodium EDTA, Glycerin, Menthol, Methylparaben, Propylene Glycol, Propylparaben, Purified Water, SD Alcohol 40-2, Symphytum Officinale (Comfrey) Leaf Extract, Triethanolamine

Package Labeling:

BED BUG INSTANT BITE RELIEF 
lidocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70466-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (LIDOCAINE) LIDOCAINE40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
CALENDULA OFFICINALIS FLOWER 
GREEN TEA LEAF 
CARBOXYPOLYMETHYLENE 
CHAMOMILE 
DIAZOLIDINYL UREA 
EDETATE DISODIUM 
GLYCERIN 
MENTHOL 
METHYLPARABEN 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
COMFREY LEAF 
TROLAMINE 
Packaging
#Item CodePackage Description
1NDC:70466-001-011 TUBE in 1 PACKAGE
128.3 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/04/2016
Labeler - P.F. Harris Mfg. Co. LLC (829811798)

 
P.F. Harris Mfg. Co. LLC

Further information

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

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