EUCALYPTAMINT- menthol ointment 
Insight Pharmaceuticals

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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Eucalyptamint
OINTMENT 16% MENTHOL®

Drug Facts

Active ingredient

Menthol 16%

Purpose

Topical Analgesic

Uses

for the temporary relief of minor aches and pains of muscles and joints associated with:

Warnings

For external use only

Do not use

  • other than as directed
  • with a heating pad or heating device

When using this product

  • avoid contact with the eyes
  • do not bandage tightly
  • do not apply to wounds or damaged skin

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

Eucalyptus Oil, Lanolin, Mineral Oil, White Petrolatum

QUESTIONS

Call 1-800-344-7239 or write to Consumer Affairs at address below.

Dist. by: INSIGHT Pharmaceuticals Corp., Langhorne, PA 19047-1749

63005H

PRINCIPAL DISPLAY PANEL - Tube Label

MAXIMUM STRENGTH

Eucalyptamint
OINTMENT 16% MENTHOL®

ARTHRITIS PAIN RELIEF FORMULA

NET WT. 2 FL. OZ. (60mL)

PRINCIPAL DISPLAY PANEL - Tube Label

PRINCIPAL DISPLAY PANEL - Carton Label

Eucalyptamint
OINTMENT 16% MENTHOL®

ARTHRITIS PAIN RELIEF FORMULA

EASY OPENING TUBE
NET WT. 2 FL. OZ. (60mL)

PRINCIPAL DISPLAY PANEL - Carton Label
EUCALYPTAMINT 
menthol ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63736-340
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A) Menthol9.6 mL  in 60 mL
Inactive Ingredients
Ingredient NameStrength
Eucalyptus Oil (UNII: 2R04ONI662)  
Mineral Oil (UNII: T5L8T28FGP)  
Petrolatum (UNII: 4T6H12BN9U)  
Product Characteristics
ColorYELLOWScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63736-340-021 in 1 BOX
160 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/09/2009
Labeler - Insight Pharmaceuticals (176792315)

Revised: 7/2009
Document Id: 2472480b-14b6-4e03-bfaf-0f8d3e4594aa
Set id: 266b1621-724a-4d44-89e5-1501d10ed973
Version: 1
Effective Time: 20090720
 
Insight Pharmaceuticals