Everflex Topical Analgesic Pain Relief with MSM

Manufacturer
Natures Sunshine Products, Inc. | Wasatch Product Development, LLC
Effective date
2021-04-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:55

Label at a glance#

ProductEverflex Topical Analgesic Pain Relief with MSM
Active ingredientMENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients                         Purpose

Menthol 1.25%                              Topical analgesic

OTC - PURPOSE SECTION

Use

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


-Keep out of reach of children

INDICATIONS & USAGE SECTION


-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 SECTION

Warnings

-For external use only
-Avoid contact with eyes

DOSAGE & ADMINISTRATION SECTION

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 SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


Everflex Topical Analgesic Pain Relief Cream with MSM

2 fl oz. (58.7 mL)

everflex 2Beverflex 2B

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
416982menthol 1.25 % Topical CreamPSN1
416982menthol 12.5 MG/ML Topical CreamSCD1
416982menthol 1.25 % Topical CreamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61582-533-012023-01-30C16284748780-1f386c649-e4b2-0266-e053-dadaa90a7c1aEverflex Topical Analgesic Pain Relief with MSM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61582-533-01Everflex Topical Analgesic Pain Relief with MSM58.7 mL in 1 JARCREAM58.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61582-533EVERFLEX TOPICAL ANALGESIC PAIN RELIEF WITH MSM (MENTHOL) CREAM [NATURES SUNSHINE PRODUCTS, INC.]1Legacy NDC, 1 package rows20210424_c098e834-dc10-0a3b-e053-2a95a90ac96f.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61582-53361582-533-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c098e83f-4da2-387c-e053-2a95a90a8c42c098e834-dc10-0a3b-e053-2a95a90ac96f2021-04-14WarningsExact identifier
spl id: c098e83f-4da2-387c-e053-2a95a90a8c42
spl set id: c098e834-dc10-0a3b-e053-2a95a90ac96f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.