Walgreens Black Elderberry Cold And Flu Relief

Bryonia Alba, Gelsemium Sempervirens, Sambucus Nigra, Sulphur, Zincum Gluconicum

Walgreen Co.
Human Otc Drug
NDC 0363-9791

Walgreens Black Elderberry Cold And Flu Relief also known as Bryonia Alba, Gelsemium Sempervirens, Sambucus Nigra, Sulphur, Zincum Gluconicum is a human otc drug labeled by 'Walgreen Co.'. National Drug Code (NDC) number for Walgreens Black Elderberry Cold And Flu Relief is 0363-9791. This drug is available in dosage form of Tablet, Orally Disintegrating. The names of the active, medicinal ingredients in Walgreens Black Elderberry Cold And Flu Relief drug includes Bryonia Alba Root - 6 [hp_X]/1 Gelsemium Sempervirens Root - 6 [hp_X]/1 Sambucus Nigra Flowering Top - 3 [hp_X]/1 Sulfur - 12 [hp_X]/1 Zinc Gluconate - 2 [hp_X]/1 . The currest status of Walgreens Black Elderberry Cold And Flu Relief drug is Active.

Drug Information:

Drug NDC:	0363-9791
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Walgreens Black Elderberry Cold And Flu Relief
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Bryonia Alba, Gelsemium Sempervirens, Sambucus Nigra, Sulphur, Zincum Gluconicum
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Walgreen Co.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Tablet, Orally Disintegrating
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	BRYONIA ALBA ROOT - 6 [hp_X]/1 GELSEMIUM SEMPERVIRENS ROOT - 6 [hp_X]/1 SAMBUCUS NIGRA FLOWERING TOP - 3 [hp_X]/1 SULFUR - 12 [hp_X]/1 ZINC GLUCONATE - 2 [hp_X]/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	13 May, 2022
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	16 Jan, 2025
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.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Walgreen Co.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UPC:	0311917009650
UPC stands for Universal Product Code.
UNII:	T7J046YI2B 639KR60Q1Q CT03BSA18U 70FD1KFU70 U6WSN5SQ1Z
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:	Copper Absorption Inhibitor [EPC] Decreased Copper Ion Absorption [PE]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
0363-9791-14	1 BLISTER PACK in 1 CARTON (0363-9791-14) / 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK	13 May, 2022	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Walgreens Black Elderberry Cold And Flu Relief

Bryonia Alba, Gelsemium Sempervirens, Sambucus Nigra, Sulphur, Zincum Gluconicum

Tablet, Orally Disintegrating
Walgreen Co.
NDC: 0363-9791

Purpose:

Purpose bryonia hpus - fever, chills, scratchy throat, muscle soreness gelsemium sempervirens hpus - sneezing, non-productive cough, bronchial irritation sambucus nigra hpus - fever, nasal congestion, coughing sulphur hpus - sinus pressure, sore throat, nasal pressure zincum gluconicum hpus - nausea, tiredness, exhaustion, bronchial constriction

Product Elements:

Walgreens black elderberry cold and flu relief bryonia alba, gelsemium sempervirens, sambucus nigra, sulphur, zincum gluconicum magnesium stearate sucrose microcrystalline cellulose european elderberry juice croscarmellose sodium zinc gluconate zinc cation lactose, unspecified form sulfur sulfur sambucus nigra flowering top sambucus nigra flowering top gelsemium sempervirens root gelsemium sempervirens root bryonia alba root bryonia alba root black carrot anthocyanins elderberry off purple off grey color with specks

Indications and Usage:

Uses* according to homeopathic indications, these ingredients provide temporary relief of cold and flu symptoms such as: nasal and sinus congestion, runny nose, sor coughing, sneezing, and chills and fever, after serious causes have been ruled out by a physician. * these statements are based upon traditional homeopathic practice. they have not been reviewed by the food and drug administration.

Warnings:

Warnings warnings a physician should always be consulted to rule out serious causes. sore throat warning - severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. consult phys do not use more than 2 days or administer to children under 4 years of age unless directed by a physician. this product is intended to complement, not replace, medical treatment. initial worsening of symptoms may occur.

Dosage and Administration:

Directions directions suitable for adults and children ages 4 and over. children under the age of 4: consult a physician before use. for best results, take at the start of the symptoms for cold or flu and continue to take for another 48 hours after the symptoms end. dissolve entire tablet under tongue or chew tablet and swallow. do not swallow tablet whole. take 1 tablet every three hours. take at least 10 minutes before or at least 10 minutes after eating or drinking. homeopathic remedies may not be effective for everyone. individual results may vary.

Stop Use:

Stop use stop use and ask a doctor if: you experience worsening symptoms. any new symptoms appear. symptoms last longer than 7 days.

Package Label Principal Display Panel:

Principal display panel carton

Further Questions:

Questions or comments? questions or comments? 1-800-925-4733 9am-5pmestmonday-friday

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.