NDC Package 66774-1001-2 Blister Blaster

View Billable Units, 11-Digit Format, RxNorm

Package Information

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

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
66774-1001-2
Package Description:
2 VIAL in 1 BLISTER PACK / .6 mL in 1 VIAL
Product Code:
Proprietary Name:
Blister Blaster
Usage Information:
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.
11-Digit NDC Billing Format:
66774100102
NDC to RxNorm Crosswalk:
  • RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
  • RxCUI: 1049254 - benzalkonium chloride 1.3 MG/ML Topical Solution
  • RxCUI: 1116098 - blisterblaster 0.13 % Topical Solution
  • RxCUI: 1116098 - benzalkonium chloride 1.3 MG/ML Topical Solution [Blister Blaster]
  • RxCUI: 1116098 - Blister Blaster 0.13 % Topical Solution
  • Labeler Name:
    Quadex Pharmaceuticals, Llc
    Sample Package:
    No
    Start Marketing Date:
    04-01-2010
    Listing Expiration Date:
    12-31-2018
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 66774-1001-2?

    The NDC Packaged Code 66774-1001-2 is assigned to a package of 2 vial in 1 blister pack / .6 ml in 1 vial of Blister Blaster, labeled by Quadex Pharmaceuticals, Llc. The product's dosage form is and is administered via form.

    Is NDC 66774-1001 included in the NDC Directory?

    No, Blister Blaster with product code 66774-1001 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Quadex Pharmaceuticals, Llc on April 01, 2010 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 66774-1001-2?

    The 11-digit format is 66774100102. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-166774-1001-25-4-266774-1001-02