NDC 67091-377 12 Hour Nasal Decongestant Extra Moisturizing

Nasal Spray

NDC Product Code 67091-377

NDC 67091-377-08

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

NDC Product Information

12 Hour Nasal Decongestant Extra Moisturizing with NDC 67091-377 is a a human over the counter drug product labeled by Winco Foods Llc. The generic name of 12 Hour Nasal Decongestant Extra Moisturizing is nasal spray. The product's dosage form is liquid and is administered via nasal form.

Labeler Name: Winco Foods Llc

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.

Product Type: Human Otc Drug 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.

12 Hour Nasal Decongestant Extra Moisturizing Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • POVIDONE K29/32 (UNII: 390RMW2PEQ)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Nasal - Administration to the nose; administered by way of the nose.

Product Labeler Information

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

Labeler Name: Winco Foods Llc
Labeler Code: 67091
FDA Application Number: part341 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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.

Start Marketing Date: 03-25-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

12 Hour Nasal Decongestant Extra Moisturizing Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Drug Facts

Active IngredientOxymetazoline Hydrochloride 0.05%


Nasal Decongestant


  • Temporarily relieves nasal congestion due to:common coldhay feversinusitisupper respirtory allergiesShrink swollen membranes so you can breathe more freely

Ask A Doctor Before Use If You Have

  • Heart dieasehigh blood pressurediabetesthyiod dieasetrouble urinating due to enlarged rostate gland.

When Using This Product

  • Do not use more than directeddo not use for more than three days, Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen.temporary discomfort such as burning ,stinging, sneezing or an increase in nasal discharge may occuruse of this container by more thna one person may spread infection.

Stop Use And Ask A Doctor If

Symptoms persist.

Keep Out Of The Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Other Information

  • Store between 20° and 25°C (68° to 77°F)retain carton for future reference on full labeling

Inactive Ingredients:

Benzalkonium chloride, edetate disodium, glycerin, polyethylene glycol, povidone, propylene glycol, sodium phosphate dibasic, sodium phosphate monobasic, water

* Please review the disclaimer below.