NDC 69512-001 Alivio Medicated Pain

  1. Labeler Index
  2. Alivio Medical Products, Llc
  3. NDC: 69512-001 Alivio Medicated Pain

NDC Product Code 69512-001

NDC CODE: 69512-001

Proprietary Name: Alivio Medicated Pain 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 69512 - Alivio Medical Products, Llc

NDC 69512-001-01

Package Description: 15 PATCH in 1 BOX > 8.5 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

Alivio Medicated Pain with NDC 69512-001 is a product labeled by Alivio Medical Products, Llc. The generic name of Alivio Medicated Pain is . The product's dosage form is and is administered via form.

Labeler Name: Alivio Medical Products, Llc

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.
  • ACRYLIC ACID (UNII: J94PBK7X8S)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
  • 2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • METHYL ACRYLATE (UNII: WC487PR91H)
  • NONOXYNOL-30 (UNII: JJX07DG188)
  • POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
  • POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • TALC (UNII: 7SEV7J4R1U)
  • TARTARIC ACID (UNII: W4888I119H)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Alivio Medical Products, Llc
Labeler Code: 69512
Start Marketing Date: 01-21-2015 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.

Alivio Medicated Pain Product Label Images

Alivio Medicated Pain 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 Ingredient

Menthol 5.00%Capsacin 0.03%

Purpose

External AnalgesicExternal Analgesic

Uses:

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

Warnings:

  • For external use only.Avoid contact with eyes.

Do Not

  • Apply to open wounds or damages skin.bandage tightlyIf symptoms persist for more than seven days, discontinue use and consult physician.

Keep Out Of Reach Of Children

If swallwed, consult physician.

If Pregnant Or Breast Feeding,

Contact physician prior to use.

Directions:

  • Clean and dry affected area.Remove patch from backing and apply to affected area.  Apply directly to effected area.Use only on patch at a time, and a maximum of four patches per day.Leave patch on affected area for up eight hours.Do not use patches for more than five consecutive days.Children under 12 should consult a physician prior to use.

Other Ingredients:

Acrylic acid ,aluminum hydroxide .carmellose sodium 2-ethylhexyl acrylate .glycerin . isopropyl myristate .methyl acrylatenonoxynol-30 .polyacrylate.polyacrylic acid .polysorbate 80 sorbitan sesquioleate starch .talc .tartaric acid. titanium dioxide. water (245-114)

Store

At room temperature.  Avoid direct sunlight

Package Label

Alivio Patch MEDICATED PAIN PATCH 15 PATCHESDistributed by:Alivio Medical ProductsHollywood, FL 33020

* Please review the disclaimer below.