ECOLYPTUS PAIN RELIEVING MUSCLE RUB- menthol cream 
Pure Source, LLC

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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:

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 Label

ECOLYPTUS PAIN RELIEVING MUSCLE RUB 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-715
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL60 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
GLYCERIN (UNII: PDC6A3C0OX)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65121-715-881 in 1 CARTON02/09/2017
188.7 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01702/06/2014
Labeler - Pure Source, LLC (080354456)
Establishment
NameAddressID/FEIBusiness Operations
Pure Source, LLC080354456manufacture(65121-715)

Revised: 11/2023
Document Id: 0974579b-6f47-6b47-e063-6294a90a0217
Set id: 2ac95778-c7c0-44a2-b906-8783a0525e47
Version: 4
Effective Time: 20231105
 
Pure Source, LLC