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dynaFreeze

Performance Health LLC

dynaFreeze


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

dynaFreeze


Active Ingredient


Purpose


Uses:



Warnings:


Ask a doctor before use if you have:

sensitive skin, are pregnant or breast feeding

When using this product:

  • Avoid contact with eyes or mucous membranes
  • Do not apply to wounds, damaged or irritated skin, or if excessive irritation develops
  • Do not bandage or use with heating pad or device, ointments, creams, sprays or liniments
  • After applying, wash hands with cool water

Stop use and ask a doctor if:

Condition worsens, symptoms persist more than 7 days, or clear up and then recur

Keep out of reach of children:


Directions:

  • Adults / Children 2 years and older: Massage onto affected area up to 4 times daily
  • Children under 2 years of age: Consult physician

Other Information:

Inactive Ingredients:

Questions or Comments?


Product Label

dynaFreeze

dynaFreeze

MENTHOL LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59316-301
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 35 mg

Inactive Ingredients

Ingredient Name Strength
water
ISOPROPYL ALCOHOL
ILEX PARAGUARIENSIS LEAF
TROLAMINE
SILICON DIOXIDE
METHYLPARABEN
GLYCERIN
propylene glycol
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59316-301-10 118 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2010-08-25


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Be sure to consult your doctor before taking any medication!
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