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Name:Apanolarthritis Extra Strength
Manufacturer:Delon Laboratories (10) Ltd
Category:Over-the-counter (OTC) Marketed Drugs


Drug Facts

APANOL ARTHRITIS EXTRA STRENGTH - menthol and 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

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 labelmm1



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 DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Menthol (Menthol) Menthol 10 g  in 100 g
Methyl Salicylate (Methyl Salicylate) Methyl Salicylate 27 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
Petrolatum 59 g  in 100 g
Paraffin 4 g  in 100 g
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:61734-201-01 99 g in 1 JAR None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part348 11/19/2010

Labeler - Delon Laboratories (1990) Ltd (248364184)
Establishment
Name Address ID/FEI Operations
Delon Laboratories (1990) Ltd 248364184 label, manufacture, pack

Revised: 11/2010 Delon Laboratories (1990) Ltd



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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