Apanol Alcanfor

Dosage form: ointment
Ingredients: Camphor (Synthetic) 10g in 100g
Labeler: Delon Laboratories (1990) Ltd
NDC Code: 61734-200

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 Ingredient
Camphor 10%

Pain Reliever

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

Warnings
  • For external use only.
  • Avoid contact with eyes, mucous membranes and broken or irritated skin.
  • Do not swallow.

Stop use and ask doctor if
  • symptoms persist for more than 2 days or if condition gets worse.

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 to children even if you don't notice any signs or symptoms.

Directions
  • Adults and children 2 years of age and older: Apply to affected area 3 to 4 times daily. Consult a physician for children under 2 years of age. Keep away from the reach of children. Store in a dry place and do not expose to temperature above 25C (77F).

    

Inactive Ingredients ‚ÄčPetrolatum

mm1


APANOL  ALCANFOR
camphor ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61734-200
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Camphor (Synthetic) (Camphor (Synthetic)) Camphor (Synthetic)10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Petrolatum90 g  in 100 g
Packaging
#Item CodePackage Description
1NDC:61734-200-0160 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34811/19/2010
Labeler - Delon Laboratories (1990) Ltd (248364184)
Establishment
NameAddressID/FEIOperations
Delon Laboratories (1990) Ltd248364184label, manufacture, pack

Revised: 11/2010
 
Delon Laboratories (1990) Ltd

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide
(web3)