EVERFLEX TOPICAL ANALGESIC PAIN RELIEF WITH MSM- menthol cream 
Natures Sunshine Products, Inc.

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 with MSM

Active Ingredients                         Purpose

Menthol 1.25%                              Topical analgesic

Use

For temporary relief of minor aches and pains associated with with simple backache, arthritis, strains, bruises and sprains.


-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

Warnings

-For external use only
-Avoid contact with eyes

Directions

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


Everflex Topical Analgesic Pain Relief Cream with MSM

2 fl oz. (58.7 mL)

everflex 2B

EVERFLEX TOPICAL ANALGESIC PAIN RELIEF WITH MSM 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61582-533
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.25 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
CETYL MYRISTATE (UNII: 7OPL833Q4D)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PEG-100 STEARATE (UNII: YD01N1999R)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
CETYL PALMITOLEATE (UNII: 962I97113K)  
CETYL OLEATE (UNII: 78K2L26L8N)  
CETYL PALMITATE (UNII: 5ZA2S6B08X)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
ETHYLPARABEN (UNII: 14255EXE39)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61582-533-0158.7 mL in 1 JAR; Type 0: Not a Combination Product04/23/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/23/2021
Labeler - Natures Sunshine Products, Inc. (809048960)
Establishment
NameAddressID/FEIBusiness Operations
Wasatch Product Development, LLC962452533manufacture(61582-533)

Revised: 4/2021
Document Id: c098e83f-4da2-387c-e053-2a95a90a8c42
Set id: c098e834-dc10-0a3b-e053-2a95a90ac96f
Version: 1
Effective Time: 20210414
 
Natures Sunshine Products, Inc.