NDC 63287-420 Shing-releev

NDC Product Code 63287-420

NDC CODE: 63287-420

Proprietary Name: Shing-releev 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

  • 63287 - Merix Pharmaceutical Corp.

NDC 63287-420-02

Package Description: 1 BOTTLE, SPRAY in 1 BOX > 60 mL in 1 BOTTLE, SPRAY (63287-420-01)

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

NDC Product Information

Shing-releev with NDC 63287-420 is a product labeled by Merix Pharmaceutical Corp.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 1292894 and 1292897.

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)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • ECHINACEA PURPUREA FLOWERING TOP (UNII: 2EMS3QFX65)

Product Labeler Information

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

Labeler Name: Merix Pharmaceutical Corp.
Labeler Code: 63287
Start Marketing Date: 07-14-2010 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: 12-31-2019 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.

Shing-releev Product Label Images

Shing-releev 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:

Benzalkanium Chloride .13%Allantoin .5%Benzyl Alcohol .5%

Uses:

For the relive of symtoms associated with shingles including pain, Burning, Itching and tingling First aid to help guard against secondary skin infection due to shingles.

Warnings:

For external used only. Not for ingestion.Do not used- in yeast infections- do not spray directly on the eyesWhen using this product, may tingle on contact.Stop used and ask doctor if - condition worsens- symptomslast more then 7 days .

Keep Out Of Reach Of Children:

If swallowget medical help or contact a Poison Control Center right away.

Directions:

Use at first sign of irritation or itching.Adults and children 12  years or older. Clean without soap.apply liberally to clean dry area free of soap or cleanser residue.

Dosage & Administration

Apply to area as needed  3-4  times daily.Do not use cotton applicator.May be used with sterile bandage after area is dry.

Other Ingredients

.Methylparaben Potassium Sorbate (natural preservative ). Propylparaben , Viracea (proprietary Echinacea purpurea extract),water (purified)

* Please review the disclaimer below.