APANOL ARTHRITIS EXTRA STRENGTH- menthol, methyl salicylate ointment
Delon Laboratories (1990) Ltd

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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Drug Facts

Active Ingredient

Methyl Salicylate 27%
Menthol 10%.

Pain Reliever

Uses

Temporary relieves minor pain associated with arthritis, joint, back and or muscle pain.

Warnings

External use only.
Avoid contact with eyes, mucous membranes and broken or irritated skin.
Do not swallow.

Keep away from reach of children

If swallowed or in case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical in case of overdose for children even if you don't notice any signs or symptoms.

Stop use and ask doctor if

irritation develops
symptoms persist for more than 2 days or if condition gets worse.

Directions

Apply generously and gently to the affected area gently 3 times daily. Soothing relief is provided for minor arthritis pain, sore, aching and strained muscles and joints and backaches.

Inactive Ingredients

Petrolatum, Paraffin.

Alcanfor label mm1

APANOL ARTHRITIS EXTRA STRENGTH
menthol, methyl salicylate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:61734-201
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 g in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	27 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
PETROLATUM (UNII: 4T6H12BN9U)	59 g in 100 g
PARAFFIN (UNII: I9O0E3H2ZE)	4 g in 100 g

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:61734-201-01	99 g in 1 JAR; Type 0: Not a Combination Product	11/19/2014	12/03/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	11/19/2010	12/03/2014

Labeler - Delon Laboratories (1990) Ltd (248364184)

Name	Address	ID/FEI	Business Operations
Establishment
Delon Laboratories (1990) Ltd		243387722	label(61734-201) , manufacture(61734-201) , pack(61734-201)

Revised: 9/2016

Document Id: 3c8c9acb-52a4-6c1c-e054-00144ff88e88

Set id: 6465a6f0-394e-4321-8928-d955396b307e

Version: 7

Effective Time: 20160915

Delon Laboratories (1990) Ltd