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  4. NDC Product Code: 70019-100 Zzip Cold Sore Treatment

NDC 70019-100 Zzip Cold Sore Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70019-100?
  4. Zzip Cold Sore Treatment 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:
70019-100
Proprietary Name:
Zzip Cold Sore Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zzip Ag
Labeler Code:
70019
Product Label ID:
cf62370a-9a10-46b1-b320-23eaf196040c
Start Marketing Date: [9]
07-30-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70019-100-00

Package Description: 3 mL in 1 TUBE

Product Details

What is NDC 70019-100?

The NDC code 70019-100 is assigned by the FDA to the product Zzip Cold Sore Treatment which is product labeled by Zzip Ag. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70019-100-00 3 ml in 1 tube . 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 Zzip Cold Sore Treatment?

​adults and children 12 years or over:​ - Apply to affected area on face or lips at first sign (tingle) of cold sore/fever blister- Open tube, saturate cotton swab with 8 drops of liquid- Use the cotton swab to apply to affeted area on face or lips. Do ot touch the sore with your fingers. Continue for 3 seconds until the cold sore is completely covered and sealed.- Dispose of cotton swab - do not reuse- Wash hands before and after application.- Apply 2 times daily, not to exceed 3 to 4 times daily until sore is healed​children under 12 years: ask a doctor

Which are Zzip Cold Sore Treatment UNII Codes?

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

Which are Zzip Cold Sore Treatment 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 Zzip Cold Sore Treatment?

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:
  • RxCUI: 1659645 - allantoin 0.5 % / dimethicone 1 % / menthol 0.1 % Topical Solution
  • RxCUI: 1659645 - allantoin 5 MG/ML / dimethicone 10 MG/ML / menthol 1 MG/ML Topical Solution
  • RxCUI: 1659650 - Zzip Cold Sore (allantoin 0.5 % / dimethicone 1 % / menthol 0.1 % ) Topical Solution
  • RxCUI: 1659650 - allantoin 5 MG/ML / dimethicone 10 MG/ML / menthol 1 MG/ML Topical Solution [Zzip]

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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".