1. Home
  2. Labeler Index
  3. Supervalu Inc
  4. NDC Product Code: 41163-716 Equaline Oxymetazoline Hcl Nasal Decongestant No Drip

NDC 41163-716 Equaline Oxymetazoline Hcl Nasal Decongestant No Drip

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 41163-716?
  5. Equaline Oxymetazoline Hcl Nasal Decongestant No Drip Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
41163-716
Proprietary Name:
Equaline Oxymetazoline Hcl Nasal Decongestant No Drip
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Supervalu Inc
Labeler Code:
41163
Product Label ID:
7f415a47-5240-41a0-b9df-217aa9a212dd
Start Marketing Date: [9]
06-12-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - TRANSLUCENT)

Product Packages

NDC Code 41163-716-01

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

Product Details

What is NDC 41163-716?

The NDC code 41163-716 is assigned by the FDA to the product Equaline Oxymetazoline Hcl Nasal Decongestant No Drip which is product labeled by Supervalu Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41163-716-01 1 bottle, spray in 1 carton / 30 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 Equaline Oxymetazoline Hcl Nasal Decongestant No Drip?

•adults and children 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period.•children under 6 years of age: ask a doctor.Shake well before use. Before using the first time, remove the protective cap from the tip by pressing and twisting off the cap. Rotate the lock tab to align arrow marks to unlock the pump. Prime metered pump by depressing pump firmly several times. To spray, hold bottle with thumb at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostril. Fully depress rim with a firm, even stroke and sniff deeply. Wipe nozzle clean after use. Lock the pump by ensuring that arrow marks are not aligned and replace the protective cap on tip.

Which are Equaline Oxymetazoline Hcl Nasal Decongestant No Drip UNII Codes?

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

Which are Equaline Oxymetazoline Hcl Nasal Decongestant No Drip 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 Equaline Oxymetazoline Hcl Nasal Decongestant No Drip?

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:

* Please review the disclaimer below.

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".