NDC 49795-227 Pro-flex

NDC Product Code 49795-227

NDC CODE: 49795-227

Proprietary Name: Pro-flex What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

NDC 49795-227-01

Package Description: 120 g in 1 JAR

NDC 49795-227-02

Package Description: 500 g in 1 BOTTLE, PLASTIC

NDC 49795-227-03

Package Description: 5 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

Pro-flex with NDC 49795-227 is a product labeled by Nutri-dyn Products Ltd. Dba Professional Health Products. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 900389.

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.

  • WATER (UNII: 059QF0KO0R)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • GLYCOL STEARATE (UNII: 0324G66D0E)
  • DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
  • C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • UREA (UNII: 8W8T17847W)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • SORBIC ACID (UNII: X045WJ989B)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • METHYL SALICYLATE (UNII: LAV5U5022Y)
  • VITAMIN E (UNII: H4N855PNZ1)
  • LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
  • THYMOL (UNII: 3J50XA376E)
  • CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
  • CUCUMARIA SEA CUCUMBER (UNII: 3SC3X5I2GC)
  • GRAPE SEED OIL (UNII: 930MLC8XGG)

Product Labeler Information

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

Labeler Name: Nutri-dyn Products Ltd. Dba Professional Health Products
Labeler Code: 49795
Start Marketing Date: 02-01-2004 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 - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Pro-flex Product Label Images

Pro-flex 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 (Percent by weight)           PurposeMenthol  4.0%  ............................Analgesic              (Pain reliever)Camphor 4.0%  ...........................Analgesic               (Pain reliever)

Indications & Usage

Uses for the temporary relief of minor aches and joint pain associated with backpain, arthritis, strains, bruises and sprains.

Warnings

  • WarningsFor external use only.  Avoid contact with eyes.  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 this product and consult a doctor.Do not apply to wounds or damaged skinDo not bandage tightly

Otc - Keep Out Of Reach Of Children

Keep out of the reach of childrenIf swallowed, get medical help or contact a poison control center right away.

Dosage & Administration

  • DirectionsAdults and children 2 years of age and older:  Apply to affected area several times daily.Children under 2 years of age:  Do not use, consult a doctor.

Inactive Ingredient

C13-14 isoparaffin, caprylyl glycol, cetyl alcohol, chondroitin sulfate, denatured alcohol, eucalyptus oil, glucosamine sulfate, glycerin, grape seed oil, laureth-7, methylsulfonylmethane (MSM), oil of lavender, oil of wintergreen, phenoxyethanol, polyacrylamide, polysorbate-20, sea cucumber extract, sorbic, acid, stearyl alcohol, thymol, urea, vitamin E, water

References

Distributed by:PROFESSIONAL HEALTH PRODUCTS4307-49th Street    Innisfail, AB  CANADA T4G 1P31-403-227-3926

Otc - Purpose

Pain Reliever

* Please review the disclaimer below.