0113-0112 NDC - GOOD SENSE NAUSEA RELIEF (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID)

Drug Information

Product NDC: 0113-0112

Proprietary Name: good sense nausea relief

Non Proprietary Name: Dextrose (glucose), Levulose (fructose), Phosphoric Acid

Active Ingredient(s):
  • 1.87 g/5mL DEXTROSE;
  • 1.87 g/5mL FRUCTOSE;
  • 21.5 mg/5mL PHOSPHORIC ACID


Administration Route(s): ORAL

Dosage Form(s): SOLUTION

Labeler Information

Labeler Name: L. Perrigo Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:11/3/2014

Package Information

No. Package Code Package Description Billing Unit
10113-0112-261 BOTTLE in 1 CARTON (0113-0112-26) > 118 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC0113-0112The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEgood sense nausea reliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEDextrose (glucose), Levulose (fructose), Phosphoric AcidThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/3/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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.
LABELER NAMEL. Perrigo CompanyName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEDEXTROSE; FRUCTOSE; PHOSPHORIC ACIDThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH1.87; 1.87; 21.5 
ACTIVE INGRED UNITg/5mL; g/5mL; mg/5mL 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 8/16/2019