NDC 71027-013 Oxymetazoline Hcl

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:
71027-013
Proprietary Name:
Oxymetazoline Hcl
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kingston Pharma Llc
Labeler Code:
71027
Start Marketing Date: [9]
03-01-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71027-013-02

Package Description: 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE

NDC Code 71027-013-17

Package Description: 1 BOTTLE in 1 CARTON / 15 mL in 1 BOTTLE

Product Details

What is NDC 71027-013?

The NDC code 71027-013 is assigned by the FDA to the product Oxymetazoline Hcl which is product labeled by Kingston Pharma Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 71027-013-02 1 bottle in 1 carton / 30 ml in 1 bottle, 71027-013-17 1 bottle in 1 carton / 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 Oxymetazoline Hcl?

Uses Temporarily relieves nasal congestion due to:common coldhay feverupper respiratory allergiessinusitisshrinks swollen nasal membrances so you can breathe more freely.

Which are Oxymetazoline Hcl UNII Codes?

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

Which are Oxymetazoline Hcl 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

[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".