NDC 46144-941 Fesi

NDC Product Code 46144-941

NDC 46144-941-15

Package Description: 15 PATCH in 1 BOX > 15 g in 1 PATCH

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

NDC Product Information

Fesi with NDC 46144-941 is a product labeled by Api Solutions Inc.. 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: 1552450.

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Labeler Information

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

Labeler Name: Api Solutions Inc.
Labeler Code: 46144
Start Marketing Date: 10-13-2014 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: 12-31-2018 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.

Fesi Product Label Images

Fesi 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

Active Ingredients

Menthol                     5.00%Capsaicin                   0.05%

Purpose

Topical AnalgesicTopical Analgesic

Uses

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

Warnings

For external use only.

When Using This Product

  • Use only as directed

Do Not Use

  • On, and avoid contact with face, scalp, eyes, mouth, and mucous membranes do not use on wounds or damaged or sensitive skin do not use in combination with any external heat source (heating pad, etc.) or for 1 hour before or after bathing or showering do not use in combination with any compression (bandage, wrap, brace, stocking, sock, or similar device or garment) do not use in combination with any other external analgesic products

Stop Use And Ask A Doctor If

  • Excessive redness, burning, swelling, irritation, or discomfort develops in the skin, eyes, mouth or mucous membranes condition worsens pain persists for more than 7 days symptoms clear up and occur again within a few days

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a doctor before use.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • Adults and children 16 years and over apply directly to affected area of pain change patch 1 to 2 times daily, or as directed by a doctor children under 16 years, ask a doctor before usinghow to apply:- clean and dry affected area - tear open pouch and remove one patch- remove protective film and apply directly to affected area of pain- reseal pouch containing unused patches after each use-
  • Wash hands with soap and water after applying

Other Ingredients:

Aqua (Deionized Water), Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Diazolidinyl Urea, Glycerine, Iodoproynyl Butylcabamate, Methylparaben, Polysorbate 80, Propylparaben, Sodium Polyacrylate, Tetrasodium EDTA.

Other

Distributed by:A.P.I SOLUTIONSDaphen, AL 36526For Questions or Comments Please Call 855-878-1489

* Please review the disclaimer below.