EUCALYPTAMINT- menthol ointment

Eucalyptamint by

Drug Labeling and Warnings

Eucalyptamint by is a Otc medication manufactured, distributed, or labeled by Insight Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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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:

• arthritis
• sore muscles
• simple backache
• strains
• sprains

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

• adults and children 2 years of age and older: gently massage a conservative amount into affected area not more than 3 to 4 times daily.
• children under 2 years of age: consult a doctor
• if thickening of product occurs, warm tube in palm of hand or run under warm water.

Other information

• store at room temperature
• see box or crimp of tube for lot number and exp. date

Inactive ingredients

Eucalyptus Oil, Lanolin, Mineral Oil, White Petrolatum

QUESTIONS

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

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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 - Carton Label

Eucalyptamint
OINTMENT 16% MENTHOL®

ARTHRITIS PAIN RELIEF FORMULA

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

INGREDIENTS AND APPEARANCE

EUCALYPTAMINT 
menthol ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63736-340
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A)	Menthol	9.6 mL  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
Eucalyptus Oil (UNII: 2R04ONI662)
Mineral Oil (UNII: T5L8T28FGP)
Petrolatum (UNII: 4T6H12BN9U)

Product Characteristics
Color	YELLOW	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63736-340-02	1 in 1 BOX
1		60 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/09/2009

Labeler - Insight Pharmaceuticals (176792315)