TopiCool Pain Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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TopiCool Pain Relief

TENSproducts, Inc.

TOPICOOL PAIN RELIEF GEL WITH CATS CLAW - Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients:

Camphor 0.4%

Menthol 4.5%

Purpose:

External Analgesic

External Analgesic

Uses:

For the temporary relief of

  • arthritis
  • backache
  • sprains
  • strains

Warnings:

Use only as directed.
For external use only.

Do not use

  • with other topical products
  • on open wounds or damaged skin

Ask a doctor or pharmacist if you are

pregnant or breastfeeding

Stop use and consult a doctor if

symptoms persist for more than 7 days


Avoid contact with eyes
Do not bandage tightly
Keep away from excessive heat or open flame

KEEP OUT OF REACH OF CHILDREN.

In case of ingestion, seek professional assistance and contact poison control immediately.

Directions:

  • Adults and children 2 years of age and older apply to affected area not more than 4 times daily
  • rub in thoroughly until gel is absorbed

Other information:

Store at room temperature with cap closed.

Inactive Ingredients:

Water, Boswellia Serrata Extract, Ethylhexylglycerin, Glycerin, Ilex Paraguariansis Extract, Isopropyl Alcohol, Phenoxyethanol, Polysorbate-20, Propylene Glycol, Tetrasodium ETDA, Triethanolamine, Uncaria Tomentosa (Cat's Claw) Extract, Zemea Propanediol.

Questions or Comments?

(866) 449-1010 or www.tensproducts.com

Principal Display Label

TopiCool Pain Relief

TopiCool Pain Relief

Menthol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57698-100
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 4.5 g
CAMPHOR (NATURAL) 0.4 g

Inactive Ingredients

Ingredient Name Strength
water
INDIAN FRANKINCENSE
ETHYLHEXYLGLYCERIN
GLYCERIN
ILEX PARAGUARIENSIS LEAF
ISOPROPYL ALCOHOL
PHENOXYETHANOL
POLYSORBATE 20
propylene glycol
EDETATE SODIUM
TROLAMINE
UNCARIA TOMENTOSA ROOT
TRIMETHYLOLPROPANE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57698-100-04 113.4 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-08-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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