NDC 62750-001 Zicam Allergy Relief

Galphimia Glauca Flowering Top, Histamine Dihydrochloride, Luffa Operculata Fruit, And Sulfur

NDC Product Code 62750-001

NDC CODE: 62750-001

Proprietary Name: Zicam Allergy Relief What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Galphimia Glauca Flowering Top, Histamine Dihydrochloride, Luffa Operculata Fruit, And Sulfur What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 62750-001-11

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 15 mL in 1 BOTTLE, PLASTIC

NDC 62750-001-12

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

NDC Product Information

Zicam Allergy Relief with NDC 62750-001 is a a human over the counter drug product labeled by Matrixx Initiatives, Inc.. The generic name of Zicam Allergy Relief is galphimia glauca flowering top, histamine dihydrochloride, luffa operculata fruit, and sulfur. The product's dosage form is spray and is administered via nasal form.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Zicam Allergy Relief 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.

  • 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: Matrixx Initiatives, Inc.
Labeler Code: 62750
Marketing Category: UNAPPROVED HOMEOPATHIC - 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: 04-14-2000 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 10-31-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Zicam Allergy Relief Product Label Images

Zicam Allergy Relief 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 Ingredients

Galphimia glauca 12x, 30xHistaminum hydrochloricum 12x, 30x, 200xLuffa operculata 4x, 12x, 30xSulphur 12x, 30x, 200x


Upper respiratory allergy symptom relief


  • Temporarily relieves symptoms due to hay fever or other upper respiratory allergies such as:sinus pressureitchy, runny nosesneezingitchy, watery eyesnasal congestion


For nasal use only.

Ask A Doctor Before Use If You Have

  • Ear, nose, or throat sensitivitysusceptibility to nosebleedsbreathing problems such as emphysema or chronic bronchitis

When Using This Product

  • Avoid contact with eyes. Rinse right away with water if it gets in eyes and seek medical help right away.the use of this container by more than one person may spread infectiontemporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge may occur

Otc - Stop Use

Stop use and ask a doctor if symptoms persist or are accompanied by fever

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


  • Adults and children 12 years of age and older:remove cap and safety clip (also see illustrations on side of carton)hold with thumb at bottom of bottle and nozzle between your fingersbefore using the first time, prime pump by depressing several timesplace tip of nozzle just past nasal opening (approximately 1/8")while inside nasal opening, slightly angle nozzle outwardpump once into each nostrilafter application, press lightly on outside of each nostril for about 5 secondswait at least 30 seconds before blowing noseuse once every 4 hoursoptimal results may not be seen for 1-2 weeks. After 1-2 weeks, you may need to use only 1-2 times daily. For best results, use up to 1 week before contact with known causes of your allergies.children under 12 years of age: ask a doctor

Other Information

  • Store between 15-29°C (59-84°F)

Inactive Ingredients

Benzalkonium chloride, benzyl alcohol, edetate disodium, glycerin, hydroxyethylcellulose, potassium chloride, potassium phosphate, purified water, sodium chloride, sodium phosphate

* Please review the disclaimer below.