Pinworm Medicine
Pyrantel Pamoate
Reese Pharmaceutical Co.
Human Otc Drug
NDC 10956-778Pinworm Medicine also known as Pyrantel Pamoate is a human otc drug labeled by 'Reese Pharmaceutical Co.'. National Drug Code (NDC) number for Pinworm Medicine is 10956-778. This drug is available in dosage form of Suspension. The names of the active, medicinal ingredients in Pinworm Medicine drug includes Pyrantel Pamoate - 144 mg/mL . The currest status of Pinworm Medicine drug is Active.
Drug Information:
| Drug NDC: | 10956-778 |
| 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: | Pinworm Medicine |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Proprietary Name Base: | Pinworm |
| The base of the Brand/Proprietary name excluding its suffix. |
| Proprietary Name Suffix: | Medicine |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. |
| 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: | Pyrantel Pamoate |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Reese Pharmaceutical Co. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Suspension |
| 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: | PYRANTEL PAMOATE - 144 mg/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: | OTC MONOGRAPH FINAL |
| 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: | 28 Sep, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 22 Dec, 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. |
| Application Number: | part357B |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| 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: | REESE PHARMACEUTICAL CO.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 199106
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 0023513618210
|
| UPC stands for Universal Product Code. |
| UNII: | 81BK194Z5M
|
| 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 |
|---|
| 10956-778-01 | 1 BOTTLE, PLASTIC in 1 CARTON (10956-778-01) / 30 mL in 1 BOTTLE, PLASTIC | 28 Sep, 2022 | N/A | No |
| 10956-778-02 | 2 BOTTLE, PLASTIC in 1 CARTON (10956-778-02) / 30 mL in 1 BOTTLE, PLASTIC | 28 Sep, 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. |
Purpose:
Purpose anthelimintic
Product Elements:
Pinworm medicine pyrantel pamoate pyrantel pamoate pyrantel citric acid monohydrate glycerin lecithin, soybean magnesium aluminum silicate methylcellulose (100 cps) povidone dimethicone sodium benzoate sodium citrate saccharin sodium sorbitol water
Indications and Usage:
Uses for the treatment of pinworns
Warnings:
Warnings do not exceed recommended dosage
When Using:
When using this product abdominal cramps, nausea, vomiting, diarrhea, headache, or dizziness sometimes occur after taking this drug. if any of these symptoms persist, consult a doctor.
Dosage and Administration:
Directions shake well before use read bottle label and package insert carefully before taking this medication treat the entire household unless otherwise advised do not repeat treatment unless directed by a doctor this product can be taken any time of day, with or without meals. it may be taken alone or with milk or fruit juice. use of a laxative is not necessary prior to, during or after medication it signs of pinworms persist after treatment, consult a doctor weight dosage (taken as a single dose) less than 25 lb. or under 2 yrs.old do not use unless directed by a doctor 25-37 lb. 1/2 teaspoonful 38-62 lb. 1 teaspoonful 63-87 lb. 1 1/2 teaspoonfuls 88-112 lb. 2 teaspoonfuls 113-137 lb. 2 1/2 teaspoonfuls 138-162 lb. 3 teaspoonfuls 163-187 lb. 3 1/2 teaspoonfuls 188 lb. and over 4 teaspoonfuls
Package Label Principal Display Panel:
Image of carton image of carton