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NDC 83243-001 Azzurx

Melissa Officinalis Leaf, Thuja Occidentalis Leaf, Geranium Maculatum, Calendula - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83243-001?
  4. Azzurx Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
83243-001
Proprietary Name:
Azzurx
Non-Proprietary Name: [1]
Melissa Officinalis Leaf, Thuja Occidentalis Leaf, Geranium Maculatum, Calendula Officinalls
Substance Name: [2]
Calendula Officinalis Flower; Geranium Maculatum Root; Melissa Officinalis Leaf; Thuja Occidentalis Leaf
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Outbreaks, Inc.
    Labeler Code:
    83243
    Product Label ID:
    9e48aaac-48c2-451d-9f6f-369e65c1c52b
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    02-13-2023
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 83243-001?

    The NDC code 83243-001 is assigned by the FDA to the product Azzurx which is a human over the counter drug product labeled by Outbreaks, Inc.. The generic name of Azzurx is melissa officinalis leaf, thuja occidentalis leaf, geranium maculatum, calendula officinalls. The product's dosage form is liquid and is administered via topical form. The product is distributed in a single package with assigned NDC code 83243-001-01 3 applicator in 1 package / .5 ml in 1 applicator. 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 Azzurx?

    Application instructionsRemove and reverse cardboard sleeve on applicator to expose swab.Crush applicator to activate by squeezing on the “X” (in AZZURX) between thumb and forefinger until you hear a snap.Rotate applicator with swab pointing downward and squeeze gently until the swab is saturated.Discard after use.At the first sign of cold sore/fever blister (tingle): Clean the area of the tingle before applying.Apply directly to face or lips at the site of the tingle.Repeat every 12 hours until all applicators are used.After cold sore/fever blister erupts (skin broken):Clean the area of the outbreak before applying.Apply directly to the affected area of the face or lips.Repeat every 24 hours as neededChildren under 12: Ask a doctor

    What are Azzurx Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Azzurx UNII Codes?

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

    • MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
    • MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219) (Active Moiety)
    • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
    • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
    • GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ)
    • GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ) (Active Moiety)
    • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
    • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (Active Moiety)

    Which are Azzurx 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:

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    Product Footnotes

    [1] 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.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [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".