OTC Medication Information: Boil Ease

BOIL EASE- benzocaine ointment
Insight Pharmaceuticals 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.

BOIL EASE ®
PAIN RELIEVING OINTMENT

Drug Facts

Active ingredient

Benzocaine 20%

Purpose

Pain Reliever

Use

for the temporary relief of pain and discomfort caused by boils

Warning

For external use only

Do not use

for more than 3 days

Ask a doctor before use if you have

boils on the lips, nose, cheeks, or forehead

When using this product

avoid contact with the eyes

Stop use and ask a doctor if

  • fever occurs
  • redness around the boil develops
  • condition worsens or does not improve
  • symptoms persist for more than 3 days
  • symptoms clear up and occur again within a few days

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Adults and children 2 years of age and older Apply to affected area no more than 2 times daily
Children under 2 years of age Consult a doctor

Other information

Keep carton for full drug facts

Inactive ingredients

anhydrous lanolin, camphor, eucalyptus oil, menthol, petrolatum, thymol, yellow wax

Questions?

call 1-800-344-7239

©2015 Distributed by: INSIGHT Pharmaceuticals LLC., Tarrytown, NY 10591

PRINCIPAL DISPLAY PANEL

28 g Tube Carton
BOIL EASE®
PAIN RELIEVING OINTMENT

BENZOCAINE 20%
NET WT 1 oz (28 g)

PRINCIPAL DISPLAY PANEL 
28 g Tube Carton
BOIL EASE® 
PAIN RELIEVING OINTMENT
BENZOCAINE 20%
NET WT 1 oz (28 g)
(click image for full-size original)
BOIL EASE
benzocaine ointment
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63736-041
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZOCAINE (BENZOCAINE) BENZOCAINE 20 g in 100 g
Inactive Ingredients
Ingredient Name Strength
LANOLIN
CAMPHOR (SYNTHETIC)
EUCALYPTUS OIL
MENTHOL
PETROLATUM
THYMOL
YELLOW WAX
Product Characteristics
Color YELLOW Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63736-041-24 24 BOX in 1 CASE contains a BOX
1 1 TUBE in 1 BOX This package is contained within the CASE (63736-041-24) and contains a TUBE
1 28 g in 1 TUBE This package is contained within a BOX and a CASE (63736-041-24)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part348 06/21/2010 06/30/2023
Labeler — Insight Pharmaceuticals LLC (055665422)

Revised: 07/2020 Insight Pharmaceuticals LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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