NDC 78371-501 Halodine Nasal Antiseptic

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:
78371-501
Proprietary Name:
Halodine Nasal Antiseptic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Halodine Llc
Labeler Code:
78371
Start Marketing Date: [9]
02-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78371-501-01

Package Description: 1 BOTTLE, SPRAY in 1 BOX / 15 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 78371-501?

The NDC code 78371-501 is assigned by the FDA to the product Halodine Nasal Antiseptic which is product labeled by Halodine Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78371-501-01 1 bottle, spray in 1 box / 15 ml in 1 bottle, spray. 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 Halodine Nasal Antiseptic?

For nasal application to skin inside of nostrils in adults and children 3 years of age and older:1. Gently blow nose to clear both nostrils. Discard tissue.2. Remove cap.3. Close one nostril and put only the tip of spray nozzle in other nostril. Aim slightly away from center of nose.4. While sniffing gently, press down the spray nozzle twice. You'll feel a light mist in your nose. Breathe out through your mouth. 5. Repeat in other nostril. Wipe spray nozzle with clean tissue and replace cap.Children under 3 years of age: Consult a doctor.

Which are Halodine Nasal Antiseptic UNII Codes?

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

Which are Halodine Nasal Antiseptic 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 Halodine Nasal Antiseptic?

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".