Morning Sickness
Symphoricarpus Racemosus,
Liddell Laboratories, Inc.
Human Otc Drug
NDC 50845-0100Morning Sickness also known as Symphoricarpus Racemosus, is a human otc drug labeled by 'Liddell Laboratories, Inc.'. National Drug Code (NDC) number for Morning Sickness is 50845-0100. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Morning Sickness drug includes Symphoricarpos Albus Fruit - 30 [hp_C]/mL . The currest status of Morning Sickness drug is Active.
Drug Information:
| Drug NDC: | 50845-0100 |
| 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: | Morning Sickness |
| 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: | Symphoricarpus Racemosus, |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Liddell Laboratories, Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Spray |
| 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: | SYMPHORICARPOS ALBUS FRUIT - 30 [hp_C]/mL
|
| 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: | 24 May, 2011 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 25 Feb, 2024 |
| 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: | 23 Dec, 2025 |
| 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: | Liddell Laboratories, Inc.
|
| 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: | 0363113050967
|
| UPC stands for Universal Product Code. |
| UNII: | 873JZU3ASZ
|
| 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. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 50845-0100-1 | 30 mL in 1 BOTTLE, SPRAY (50845-0100-1) | 24 May, 2011 | 25 Feb, 2024 | 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. |
Purpose:
Indications: temporary relief of symptoms associated with morning sickness: nausea and vomiting, gastric problems, depressed appetite.** **these statements are based upon traditional homeopathic practice. they have not been reviewed by the food and drug administration.
Product Elements:
Morning sickness symphoricarpus racemosus, symphoricarpos albus fruit symphoricarpos albus fruit water alcohol
Indications and Usage:
Indications: temporary relief of symptoms associated with morning sickness: nausea and vomiting, gastric problems, depressed appetite.** **these statements are based upon traditional homeopathic practice. they have not been reviewed by the food and drug administration.
Warnings:
Warnings: if symptoms persist, consult a doctor. if pregnant or breast feeding, ask a doctor before use. keep out of reach of children. in case of overdose, get medical help or call a poison control center right away. do not use if tamper evident seal around neck of bottle is missing or broken.
Dosage and Administration:
Directions: for adult use only. spray twice under the tongue 3 times per day as needed.
Package Label Principal Display Panel:
Package label display: oral sprays liddell laboratories 36 msi morning sickness homeopathic 1.0 fl. oz. (30 ml) morning sickness
Further Questions:
Questions: dist. by liddell laboratories inc. woodbine, ia 51579 www.liddell.net 1-800-460-7733