NDC 62750-080 Zicam Cold Remedy Medicated Fruit Drops

Zinc Acetate Anhydrous And Zinc Gluconate

NDC Product Code 62750-080

NDC CODE: 62750-080

Proprietary Name: Zicam Cold Remedy Medicated Fruit Drops 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: Zinc Acetate Anhydrous And Zinc Gluconate 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.

Product Characteristics

ORANGE (C48331)
Shape: ROUND (C48348)
24 MM
Score: 1
ORANGE (C73406)

NDC Code Structure

  • 62750 - Matrixx Initiatives, Inc.
    • 62750-080 - Zicam Cold Remedy Medicated Fruit Drops

NDC 62750-080-10

Package Description: 25 BAR, CHEWABLE in 1 BOTTLE

NDC Product Information

Zicam Cold Remedy Medicated Fruit Drops with NDC 62750-080 is a a human over the counter drug product labeled by Matrixx Initiatives, Inc.. The generic name of Zicam Cold Remedy Medicated Fruit Drops is zinc acetate anhydrous and zinc gluconate. The product's dosage form is bar, chewable and is administered via oral form.

Dosage Form: Bar, Chewable - A solid dosage form usually in the form of a rectangle that is meant to be chewed.

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 Cold Remedy Medicated Fruit Drops 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.

  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
  • WATER (UNII: 059QF0KO0R)
  • SUCROSE (UNII: C151H8M554)

Administration Route(s)

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

  • Oral - Administration to or by way of the mouth.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)

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: 03-25-2019 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: 06-30-2022 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 Cold Remedy Medicated Fruit Drops Product Label Images

Zicam Cold Remedy Medicated Fruit Drops 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

Distributed by MatrixxInitiatives, Inc., Scottsdale, AZ85260.

Active Ingredients (In Each Medicated Drop)

Zincum aceticum 2xZincum gluconicum 2x


Reduces duration and severity of the common cold


  • Reduces duration of the common coldhelps reduce severity of cold symptoms:sore throatstuffy nosesneezingcoughingnasal congestionZicam® Cold Remedy was formulated to shorten the duration of the common cold and was not formulated to be effective for flu or allergies.

Otc - Ask Doctor

Ask a doctor before use if you have a sensitivity to zinc or are allergic to zinc

Otc - Stop Use

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

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. In case of overdose, get medical help or contact a Poison Control Center right away.


  • For best results, use at the first sign of a cold and continue to use until symptoms completely subsideadults and children 12 years of age and older:take one medicated drop at onset of symptomschew slowly and dissolve completely before swallowingrepeat every 2 – 3 hours, not to exceed 7 medicated drops in 24 hours. Take until symptoms are gone.to avoid minor stomach upset, do not take on an empty stomachdo not eat or drink for 15 minutes after use. Do not eat or drink citrus fruits or juices for 30 minutes before or after use. Otherwise, drink plenty of fluids.children under 12 years of age: ask a doctor before use

Other Information

  • Store between 15-29°C (59-84°F)avoid freezing and excessive heat

Inactive Ingredients

Citric acid, corn syrup, dextrose, dicalcium phosphate, disodium phosphate, FD&C Red #40, FD&C Yellow #6, malic acid, menthol, natural flavors, pectin, purified water, sodium citrate, sodium polyphosphate, sucralose, sucrose

* Please review the disclaimer below.