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  4. NDC Product Code: 66774-1001 Blister Blaster

NDC 66774-1001 Blister Blaster

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 66774-1001?
  4. Blister Blaster Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
66774-1001
Proprietary Name:
Blister Blaster
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Quadex Pharmaceuticals, Llc
Labeler Code:
66774
Product Label ID:
3481c8f5-6efe-4e57-b562-50385262f47b
Start Marketing Date: [9]
04-01-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 66774-1001?

The NDC code 66774-1001 is assigned by the FDA to the product Blister Blaster which is product labeled by Quadex Pharmaceuticals, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66774-1001-2 2 vial in 1 blister pack / .6 ml in 1 vial. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Blister Blaster?

Using only warm water and a washcloth, clean the lip area of any lip preparations, lotions, ointments, residual beverages, or cosmetics, including lipstick.Remove the cardboard cap from the applicator end and place the cardboard cap onto the glass/plastic vial end, opposite the brush end of the product.Squeeze the cardboard cap to break open the inner glass vial.Saturate the applicator end with solution by holding the brush end down and squeezing the container until you can see liquid on the brush applicator.For best results, massage the solution into the cold sore by rubbing. Rub firmly, but take care not to damage the tissue. The purpose of the rubbing is to deliver the drug to the infection site. Hold the vial so the solution flows to the sore.To treat most cold sores, usually one treatment is enough. If your symptoms go away and then return later, apply another dose for the second cold sore.Do not use more than 3 times per day.Children under 2 years of age — ask a doctor.Discard after use.

Which are Blister Blaster UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Blister Blaster Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Blister Blaster?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".