NDC 51715-001 Lidocoll

  1. Labeler Index
  2. Innocoll Pharmaceuticals
  3. NDC: 51715-001 Lidocoll

NDC Product Code 51715-001

NDC CODE: 51715-001

Proprietary Name: Lidocoll 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

  • 51715 - Innocoll Pharmaceuticals

NDC 51715-001-01

Package Description: 115 g in 1 BOTTLE, SPRAY

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

NDC Product Information

Lidocoll with NDC 51715-001 is a product labeled by Innocoll Pharmaceuticals. The generic name of Lidocoll is . The product's dosage form is and is administered via form.

Labeler Name: Innocoll Pharmaceuticals

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.
  • WATER (UNII: 059QF0KO0R)
  • BENZETHONIUM CHLORIDE (UNII: PH41D05744)
  • HYDROCHLORIC ACID (UNII: QTT17582CB)
  • FISH (UNII: 1PIO77PW2X)

Product Labeler Information

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

Labeler Name: Innocoll Pharmaceuticals
Labeler Code: 51715
Start Marketing Date: 01-01-2011 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.

Lidocoll Product Label Images

Lidocoll 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

Lidocaine HCl 4%...............Anesthetic

Purpose

Anasthetic

Warning

Keep out of reach of children

Avoid contact with eyes. If conditionworsens, or if symptoms persist formore than 7 days or clear up andoccur again within a few days,discontinue use and consult a doctor.Keep out of reach of children.

Use

For the temporary relief of pain anditching associated with minor burns,sunburn, minor cuts, scrapes, insectbites or minor skin irritations.

Directions

Adults and children 2 years of ageand older: Apply Lidocoll spray notmore than 3 to 4 times per day ormoisten dressing prior to removalto reduce pain.Children under 2 years of ageconsult a doctor.

Inactive Ingredients

Hydrolyzed fish collagen (15%),purified water, benzethoniumchloride and HCl.

* Please review the disclaimer below.