NDC 44717-532 Natures Sunshine Products Everflex Topical Analgesic Pain Relief

NDC Product Code 44717-532

NDC 44717-532-01

Package Description: 57 g in 1 JAR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Natures Sunshine Products Everflex Topical Analgesic Pain Relief with NDC 44717-532 is a product labeled by Wasatch Product Development, Llc. The generic name of Natures Sunshine Products Everflex Topical Analgesic Pain Relief is . The product's dosage form is and is administered via form.

Labeler Name: Wasatch Product Development, Llc

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)
  • OLIVE OIL (UNII: 6UYK2W1W1E)
  • CETYL MYRISTATE (UNII: 7OPL833Q4D)
  • MENTHOL (UNII: L7T10EIP3A)
  • 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)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Wasatch Product Development, Llc
Labeler Code: 44717
Start Marketing Date: 08-13-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Natures Sunshine Products Everflex Topical Analgesic Pain Relief Product Label Images

Natures Sunshine Products Everflex Topical Analgesic Pain Relief Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active Ingredients                         PurposeMenthol 1.25%                              Topical analgesic

Otc - Purpose

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.

Otc - 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 tightlyOther Information: Store in a cool, dry place.

Warnings

-For external use only-Avoid contact with eyes

Dosage & Administration

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

Inactive Ingredient

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.

* Please review the disclaimer below.