Friday, October 7, 2016

La Vaquita Extra Strength





Dosage Form: ointment
Drug Facts

Active Ingredient



  • Methyl Salicylate 12%

  • Menthol 3%

  • Camphor 2%

  • Eucalyptus Oil 1%


  • Pain Reliever

  • Pain Reliever

  • Pain Reliever

  • Pain Reliever


Uses


  • Provides temporary relief from minor aches and pains associated with back-aches, arthritis, sore aching and strained muscles and joints.


Warnings


● External use only.  Avoid Contact with eyes mucous membranes and broken or irritated skin. Do not swallow. Do not use if allergic to salicylates.  Do not bandage. Do not apply external heat to the application area.

Keep away from reach of children





  • Stop use and ask a doctor if:


    • pain persists or irritation develops.



Directions


  • Apply generously and gently massage affected area. Repeat 3 times daily. For children under 2 years of age consult a physician.


    

Inactive Ingredients


Petrolatum, Paraffin, Lanolin, D and C Red 17.











LA VAQUITA  EXTRA STRENGTH
methyl salicylate  ointment










Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)61734-090
Route of AdministrationTOPICALDEA Schedule    

















Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL)MENTHOL3 g  in 100 g
Methyl Salicylate (Methyl Salicylate)Methyl Salicylate12 g  in 100 g
CAMPHOR (SYNTHETIC) (CAMPHOR (SYNTHETIC))CAMPHOR (SYNTHETIC)2 g  in 100 g
EUCALYPTUS OIL (EUCALYPTUS OIL)EUCALYPTUS OIL1 g  in 100 g












Inactive Ingredients
Ingredient NameStrength
PETROLATUM75 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


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
161734-090-0190 g In 1 CANNone
261734-090-02100 g In 1 JARNone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34811/07/2010


Labeler - Delon Laboratories (1990) Ltd (248364184)









Establishment
NameAddressID/FEIOperations
Delon Laboratories (1990) Ltd248364184label, manufacture, pack
Revised: 11/2010Delon Laboratories (1990) Ltd



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