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Name:Natures Sunshine Productseverflex Topical Analgesic Pain Relief
Manufacturer:Wasatch Product Development, Llc
Category:Over-the-counter (OTC) Marketed Drugs


Everflex Topical Analgesic Pain Relief Cream

NATURES SUNSHINE PRODUCTS EVERFLEX TOPICAL ANALGESIC PAIN RELIEF - menthol cream 
Wasatch Product Development, LLC

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.

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Everflex Topical Analgesic Pain Relief Cream

Active Ingredients                         Purpose

Menthol 1.25%                              Topical analgesic

Everflex pain relief cream provides temporary relief from aching joints and the surrounding tissues. Ever flex contains a proprietary blend of esterified fatty acids which is clinically proven to provide arthritis relief, plus MSM.


-Keep out of reach of children


-If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of product and consult a physician

-Do not apply to wounds or damaged skin

-Do not bandage tightly


Other Information: Store in a cool, dry place.

-For external use only

-Avoid contact with eyes

Directions for use: Massage Everflex into painful areas 3 to 4 times per day.

Inactive Ingredients: Water, Glyceryl Stearate, Glycerin, Methylsulfonylmethane (MSM), Cetyl Myristoleate, Olea Europaea (Olive) Fruit Oil, Cetyl Myristate, Lecithin, Menthol, Tocopheryl Acetate, Benzyl Alcohol, Phenoxyethanol, Carbomber, PEG-100 Stearate, Potassium Hydroxide, Cetyl Palmitoleate, Cetyl Oleate, Cetyl Palmitate, Cetyl Laurate, Methylparaben, Propylparaben, Ethylparaben, Butylparaben, Isobutylparaben.

image of back label



Everflex Topical Analgesic Pain Relief Cream with MSM

2 Oz. (57 Grams)



Image of front label


NATURES SUNSHINE PRODUCTS  EVERFLEX TOPICAL ANALGESIC PAIN RELIEF
menthol cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:44717-532
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (MENTHOL) MENTHOL 1.25 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
GLYCERYL MONOSTEARATE  
GLYCERIN  
CETYL MYRISTOLEATE  
OLIVE OIL  
CETYL MYRISTATE  
MENTHOL  
BENZYL ALCOHOL  
PHENOXYETHANOL  
PEG-100 STEARATE  
POTASSIUM HYDROXIDE  
CETYL PALMITOLEATE  
CETYL OLEATE  
CETYL PALMITATE  
METHYLPARABEN  
PROPYLPARABEN  
ETHYLPARABEN  
BUTYLPARABEN  
ISOBUTYLPARABEN  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:44717-532-01 57 g in 1 JAR None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 08/13/2010

Labeler - Wasatch Product Development, LLC (962452533)
Registrant - Nature's Sunshine Products, Inc. (081832388)
Establishment
Name Address ID/FEI Operations
Wasatch Product Development, LLC 962452533 manufacture

Revised: 03/2011 Wasatch Product Development, LLC



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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