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ecolyptus pain relieving muscle rub

Medically reviewed on February 10, 2017

Dosage form: cream
Ingredients: MENTHOL 60mg in 1mL
Labeler: Pure Source, LLC
NDC Code: 65121-715

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.

ecolyptus pain relieving muscle rub

ecolyptus pain relieving muscle rub


Active Ingredients

Menthol 6.0%

Purpose

External Analgesic

Uses

Temporary relief from minor aches and pains of sore muscles and joints associated with:

  • arthritis
  • backache
  • strains
  • sprains

Warnings

For external use only.

Do Not:
  • Get into eyes or mucous membranes
  • Apply to wounds or damaged skin
  • Bandage

Stop use and consult a physician if:

Condition worsens, or if symptoms persist for more than 7 days, or clear up and recur.

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions:

For adults and children 2 years and older: Apply to affected area up to 4 times daily. For children under 2 years of age: Consult a physician.

Inactive Ingredients:

Aqua [Deionized Water], Caprylic/Capric Triglyceride, Cetearyl Olivate, Citric Acid, Eucalyptus Globulus Oil, Gluconolactone, Glycerin, Potassium Sorbate, SD-Alcohol 38B, Sodium Benzoate, Sorbitan Olivate, Xanthan Gum

ecolyptus pain relieving muscle rub 88.7ml (65121-715-88)

ECOLYPTUS PAIN RELIEVING MUSCLE RUB 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-715
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL60 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
MEDIUM-CHAIN TRIGLYCERIDES 
CETEARYL OLIVATE 
CITRIC ACID MONOHYDRATE 
EUCALYPTUS OIL 
GLUCONOLACTONE 
GLYCERIN 
POTASSIUM SORBATE 
SODIUM BENZOATE 
SORBITAN OLIVATE 
XANTHAN GUM 
Packaging
#Item CodePackage Description
1NDC:65121-715-881 TUBE in 1 CARTON
188.7 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/06/2014
Labeler - Pure Source, LLC (080354456)
Establishment
NameAddressID/FEIOperations
Pure Source, LLC080354456manufacture(65121-715), repack(65121-715)

 
Pure Source, LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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