EVERFLEX TOPICAL ANALGESIC PAIN RELIEF WITH MSM- menthol cream

Everflex Topical Analgesic Pain Relief with MSM by

Drug Labeling and Warnings

Everflex Topical Analgesic Pain Relief with MSM by is a Otc medication manufactured, distributed, or labeled by Natures Sunshine Products, Inc., Wasatch Product Development, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients                         Purpose

Menthol 1.25%                              Topical analgesic

PURPOSE

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

-Keep out of reach of children

INDICATIONS & USAGE

-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

Warnings

-For external use only
-Avoid contact with eyes

DOSAGE & ADMINISTRATION

Directions

• Adults and children 2 yrs of age and and older. Apply to affected area not more than 3 to 4 times per day.
• Children under 2 yrs of age: Consult a physician

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

Everflex Topical Analgesic Pain Relief Cream with MSM

2 fl oz. (58.7 mL)

INGREDIENTS AND APPEARANCE

EVERFLEX TOPICAL ANALGESIC PAIN RELIEF WITH MSM 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61582-533
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1.25 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61582-533-01	58.7 mL in 1 JAR; Type 0: Not a Combination Product	04/23/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/23/2021

Labeler - Natures Sunshine Products, Inc. (809048960)

Establishment
Name	Address	ID/FEI	Business Operations
Wasatch Product Development, LLC		962452533	manufacture(61582-533)