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Mentholatum

Dosage form: ointment
Ingredients: CAMPHOR (SYNTHETIC) 90mg in 1g, MENTHOL, UNSPECIFIED FORM 13mg in 1g
Labeler: The Mentholatum Company
NDC code: 10742-0001

Drug Facts

Active ingredients

Camphor 9%

Menthol, natural 1.3%

Purpose

Camphor - Topical Analgesic

Menthol, natural - Topical Analgesic

Uses

temporarily relieves minor aches and pains of muscles and joints

Warnings

For external use only

When using this product
•
do not heat
•
do not microwave
•
do not add to hot water or any container where heating water. May cause splattering and result in burns.
•
do not get into eyes
•
do not apply to wounds or to damaged skin
•
do not bandage tightly

Stop use and ask a doctor if
•
condition worsens
•
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 and over: apply to affected area not more than 3 to 4 times daily
•
children under 2 years: ask a doctor

Inactive ingredients

fragrance, petrolatum, titanium dioxide

Questions?

Toll free 1-877-636-2677 MON-FRI 9AM to 5PM (EST)

www.mentholatum.com

Package/Label Principal Display Panel
MENTHOLATUM 
camphor, menthol ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-0001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (CAMPHOR (SYNTHETIC)) CAMPHOR (SYNTHETIC)90 mg  in 1 g
MENTHOL, UNSPECIFIED FORM (MENTHOL) MENTHOL, UNSPECIFIED FORM13 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM 
TITANIUM DIOXIDE 
Packaging
#Item CodePackage Description
1NDC:10742-0001-11 JAR in 1 CARTON
128 g in 1 JAR
2NDC:10742-0001-21 JAR in 1 CARTON
285 g in 1 JAR
3NDC:10742-0001-31 TUBE in 1 CARTON
328 g in 1 TUBE
4NDC:10742-0001-41 JAR in 1 CARTON
4106.3 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/13/197612/31/2017
Labeler - The Mentholatum Company (002105757)

Revised: 12/2016
Document Id: 83a1534a-79e1-45db-b6f4-e4921183156c
Set id: 0c633ac9-7cc4-477d-8296-2a891ed4a867
Version: 5
Effective Time: 20161206
 
The Mentholatum Company

Further information

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

Medical Disclaimer