NDC 11822-1181 Rite Aid Ultra Zinc Cold Therapy

Zincum Gluconicum Tablet, Chewable Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
11822-1181
Proprietary Name:
Rite Aid Ultra Zinc Cold Therapy
Non-Proprietary Name: [1]
Zincum Gluconicum
Substance Name: [2]
Zinc Gluconate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Rite Aid Corporation
    Labeler Code:
    11822
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    04-15-2020
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325)
    Shape:
    ROUND (C48348)
    Size(s):
    15 MM
    Imprint(s):
    RP118
    Score:
    1
    Flavor(s):
    ORANGE (C73406 - CREAM)

    Product Packages

    NDC Code 11822-1181-8

    Package Description: 18 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

    Product Details

    What is NDC 11822-1181?

    The NDC code 11822-1181 is assigned by the FDA to the product Rite Aid Ultra Zinc Cold Therapy which is a human over the counter drug product labeled by Rite Aid Corporation. The generic name of Rite Aid Ultra Zinc Cold Therapy is zincum gluconicum. The product's dosage form is tablet, chewable and is administered via oral form. The product is distributed in a single package with assigned NDC code 11822-1181-8 18 tablet, chewable in 1 bottle, plastic . 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 Rite Aid Ultra Zinc Cold Therapy?

    ▪for best results, use at the first sign of a cold and continue to use as directed▪adults and children 12 years of age and older:▪chew one tablet completely at the onset of symptoms. Do not swallow tablets whole.▪repeat every 3 hours until symptoms are gone▪to avoid minor stomach upset, do not take on an empty stomach.▪do 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.▪recommended daily dose is 6 tablets for adults and 4 tablets for ages 12 through 17▪Children under 12 years of age: Consult a doctor before use.

    What are Rite Aid Ultra Zinc Cold Therapy Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Rite Aid Ultra Zinc Cold Therapy UNII Codes?

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

    Which are Rite Aid Ultra Zinc Cold Therapy 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:

    Which are the Pharmacologic Classes for Rite Aid Ultra Zinc Cold Therapy?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] 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.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] 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.

    [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".