Medication Guide App

La Vaquita Extra Strength

Generic Name: menthol, methyl salicylate, camphor (synthetic) and eucalyptus oil
Dosage Form: ointment

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%
  • 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


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  • 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.

mm1


LA VAQUITA  EXTRA STRENGTH
methyl salicylate ointment
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:61734-090
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (MENTHOL) MENTHOL 3 g  in 100 g
Methyl Salicylate (Methyl Salicylate) Methyl Salicylate 12 g  in 100 g
CAMPHOR (SYNTHETIC) (CAMPHOR (SYNTHETIC)) CAMPHOR (SYNTHETIC) 2 g  in 100 g
EUCALYPTUS OIL (EUCALYPTUS OIL) EUCALYPTUS OIL 1 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
PETROLATUM 75 g  in 100 g
PARAFFIN 7 g  in 100 g
LANOLIN 0.001 g  in 100 g
D&C RED NO. 17 0.0021 g  in 100 g
Packaging
# Item Code Package Description
1 NDC:61734-090-01 90 g in 1 CAN
2 NDC:61734-090-02 100 g in 1 JAR
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part348 11/07/2010
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



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