| Drug NDC: | 73421-2968 |
| 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: | Total Flu Cld 1 |
| 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: | Arsenicum Alb, Baptisia, Bryonia, Causticum, Cinchona, Dulcamara, Echinacea Purp, Eucalyptus, Eupatorium Perf, Gelsemium, Influenzinum, Lachesis, Phytolacca, Rhus Tox, Sarcolacticum Ac, Sulphur, Wyethia, Anas Barbariae |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | White Manufacturing Inc. Dba Micro-west |
| Name of Company corresponding to the labeler code segment of the ProductNDC. | |
| Dosage Form: | Liquid |
| 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: | ARSENIC TRIOXIDE - 10 [hp_X]/29.6mL BAPTISIA TINCTORIA ROOT - 10 [hp_X]/29.6mL BRYONIA ALBA ROOT - 10 [hp_X]/29.6mL CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE - 35 [hp_C]/29.6mL CAUSTICUM - 10 [hp_X]/29.6mL CINCHONA BARK - 10 [hp_X]/29.6mL ECHINACEA PURPUREA - 10 [hp_X]/29.6mL EUCALYPTUS GLOBULUS LEAF - 10 [hp_X]/29.6mL EUPATORIUM PERFOLIATUM FLOWERING TOP - 10 [hp_X]/29.6mL GELSEMIUM SEMPERVIRENS ROOT - 10 [hp_X]/29.6mL Load more... INFLUENZA A VIRUS - 10 [hp_X]/29.6mL LACHESIS MUTA VENOM - 10 [hp_X]/29.6mL LACTIC ACID, L- - 10 [hp_X]/29.6mL PHYTOLACCA AMERICANA ROOT - 10 [hp_X]/29.6mL SOLANUM DULCAMARA TOP - 10 [hp_X]/29.6mL SULFUR - 10 [hp_X]/29.6mL TOXICODENDRON PUBESCENS LEAF - 10 [hp_X]/29.6mL WYETHIA HELENIOIDES ROOT - 10 [hp_X]/29.6mL |
| 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 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: | 01 Jun, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 14 May, 2026 |
| 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. | |
| Manufacturer Name: | White Manufacturing Inc. DBA Micro-West |
| 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. | |
| UNII: | S7V92P67HO 5EF0HWI5WU T7J046YI2B RN2HC612GY DD5FO1WKFU 292E43P4I9 QI7G114Y98 S546YLW6E6 1W0775VX6E 639KR60Q1Q Load more... R9HH0NDE2E VSW71SS07I F9S9FFU82N 11E6VI8VEG KPS1B1162N 70FD1KFU70 6IO182RP7A J10PD1AQ0N |
| 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. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 73421-2968-1 | 29.6 mL in 1 BOTTLE (73421-2968-1) | 01 Jun, 2021 | 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. | ||||
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