La Vaquita New Extra

Dosage form: ointment
Ingredients: Methyl Salicylate 12g in 100g, MENTHOL 3g in 100g
Labeler: Delon Laboratories (1990) Ltd
NDC Code: 61734-301

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
  • Methyl Salicylate 12%
  • Menthol 3%

  • Pain Reliever
  • Pain Reliever

Uses
  • Provides temporary relief from minor aches and pains associated with backaches, arthritis, sore and strained muscles and joints.

Warnings‚óŹ External use only.  Avoid Contact with eyes and broken or irritated skin.  Do not use if allergic to salicylates.  Do not bandage. Do not apply external heat to the application area. If swallowed, get medical help or contact a Poison Control Center right away.

Keep away from reach of children


  • Stop use and ask a doctor if:
    condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Directions
  • Adults and children 2 years of age and older: Apply generously and gently massage affected area no more than 3-4 times daily. For children under 2 years of age consult a physician.
    

Inactive IngredientsPetrolatum, Paraffin, Lanolin, and D and C Red 17.

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LA VAQUITA  NEW EXTRA
methyl salicylate, menthol ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61734-301
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Methyl Salicylate (Methyl Salicylate) Methyl Salicylate12 g  in 100 g
MENTHOL (MENTHOL) MENTHOL 3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM78 g  in 100 g
PARAFFIN7 g  in 100 g
LANOLIN0.001 g  in 100 g
D&C RED NO. 170.0021 g  in 100 g
Packaging
#Item CodePackage Description
1NDC:61734-301-0190 g in 1 CAN
2NDC:61734-301-02100 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/26/2011
Labeler - Delon Laboratories (1990) Ltd (248364184)
Establishment
NameAddressID/FEIOperations
Delon Laboratories (1990) Ltd248364184label, manufacture, pack

Revised: 06/2011
 
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.

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