MENTHOLATUM ORIGINAL- camphor, menthol ointment
The Mentholatum Company

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.

----------

Drug Facts

Active ingredients

Camphor 9%

Menthol 1.3%

Purpose

Camphor - Topical Analgesic

Menthol - Topical Analgesic

Uses

temporarily relieves minor aches and pains of muscles and joints

Warnings

For external use only

When using this product

do not get into eyes
do not apply to wounds or to damaged skin
do not bandage tightly
do not heat, microwave, or add to hot water as this may cause splattering and result in burns

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?

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

Package/Label Principal Display Panel

MENTHOLATUM ORIGINAL
camphor, menthol ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10742-0002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	90 mg in 1 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	13 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
PETROLATUM (UNII: 4T6H12BN9U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:10742-0002-1	1 in 1 CARTON	12/01/2014
1		28 g in 1 JAR; Type 0: Not a Combination Product
2	NDC:10742-0002-2	1 in 1 CARTON	12/01/2014
2		85 g in 1 JAR; Type 0: Not a Combination Product
3	NDC:10742-0002-3	1 in 1 CARTON	10/19/2020
3		34 g in 1 JAR; Type 0: Not a Combination Product
4	NDC:10742-0002-4	1 in 1 CARTON	10/19/2020
4		102.1 g in 1 JAR; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	12/01/2014

Labeler - The Mentholatum Company (002105757)

Registrant - The Mentholatum Company (002105757)

Name	Address	ID/FEI	Business Operations
Establishment
The Mentholatum Company		002105757	manufacture(10742-0002)