NDC 82529-001 Vortex Moisturizer Oral

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82529-001
Proprietary Name:
Vortex Moisturizer Oral
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
82529
Start Marketing Date: [9]
03-01-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82529-001?

The NDC code 82529-001 is assigned by the FDA to the product Vortex Moisturizer Oral which is product labeled by Vortex Life Sciences, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82529-001-01 1 bottle in 1 box / 15 ml in 1 bottle. 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 Vortex Moisturizer Oral?

12 years old - adult: 3 sprays. 6 - 12 years old: 2 sprays. 3 - 6 years old: 1 spray. Children under age 3: 1 spray. Consult a physician. To use, remove cap, depress the pump completely to spray directly into mouth and throat. Day 1: every 3 hours Day 2: every 3 hours Day 3: 3 times a day Day 4: at bedtime Day 5: at bedtime Day 6 - 9: skip Day 10: at bedtime (final dose) For moderate to severe symptoms every 3 hours (minimum 5 doses/24hrs) until symptoms have significantly reduced. Then, resume at day 3 schedule.

Which are Vortex Moisturizer Oral UNII Codes?

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

Which are Vortex Moisturizer Oral 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 Vortex Moisturizer Oral?

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".