FDA.reportPublic FDA data

Emetrol Cherry

Manufacturer
Preferred Pharmaceuticals, Inc
Effective date
2012-04-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:31:33

Label at a glance#

ProductEmetrol Cherry
Active ingredientSUCROSE, PHOSPHORIC ACID
Label structure11 sections

Indications and uses

For relief of upset stomach associated with nausea due to overindulgence in food and drink.

Dosage and administration

For maximum effectiveness never dilute or drink fluids of any kind immediately before or after taking this product adults and children 12 years of age and over: one to two tablespoons children 2 to under 12: one or two teaspoons repeat dose every 15 minutes or until distress subsides do not take more than 5 doses in 1 hour without consulting a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Phosphorated carbohydrate solution*
    *each 5 mL contains:
        • 3.74 g Total sugar
        • 21.5 mg Phosphoric acid

Purpose

OTC - PURPOSE SECTION

Upset Stomach Reliever       

Uses

INDICATIONS & USAGE SECTION

For relief of upset stomach associated with nausea due to overindulgence in food and drink.

Warnings

WARNINGS SECTION

  • This product contains fructose and should not be taken by persons with hereditary fructose intolerance (HFI).

Do not use if you have

OTC - DO NOT USE SECTION

  • allergic reactions to any of the ingredients in this product

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • diabetes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • symptoms persist, return or get worse

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

  • For maximum effectiveness never dilute or drink fluids of any kind immediately before or after taking this product
  • adults and children 12 years of age and over: one to two tablespoons
  • children 2 to under 12: one or two teaspoons
  • repeat dose every 15 minutes or until distress subsides
  • do not take more than 5 doses in 1 hour without consulting a doctor

Other information

SPL UNCLASSIFIED SECTION

  • Store between 20-25ºC (68-77ºF) away from heat and direct light; keep from freezing
  • Do not use if printed foil seal under bottle cap is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

FD&C red no. 40, flavors, glycerin, methylparaben, and purified water.

How Supplied

SPL UNCLASSIFIED SECTION

118cc – 68788-9801-1

Questions or Comments?

SPL UNCLASSIFIED SECTION

call 1-866-337-4500

Distributed By

SPL UNCLASSIFIED SECTION

WellSpring Pharmaceutical Corporation
Sarasota, FL 34243 USA
(c) WellSpring 2009

Relabeled By Preferred Pharmaceuticals, Inc

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Emetrol for Nausea label
Emetrol for Nausea label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
318146dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG in 5 mL Oral SolutionPSN1
809602Emetrol 1.87 GM / 1.87 GM / 21.5 MG in 5 mL Oral SolutionPSN1
809602fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral Solution [Emetrol]SBD1
318146fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral SolutionSCD1
318146dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG per 5 ML Oral SolutionSY1
809602Emetrol (dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG) per 5 ML Oral SolutionSY1
809602Emetrol (sucrose 3.74 GM / phosphoric acid 21.5 MG) per 5 ML Oral SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68788-9801-12019-11-13C16284748780-197449f38-b693-f6ea-e053-dbdaa90aa703Emetrol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68788-9801-1Emetrol Cherry118 mL in 1 BOTTLESOLUTION1181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-9801EMETROL CHERRY (PHOSPHORATED CARBOHYDRATE) SOLUTION [PREFERRED PHARMACEUTICALS, INC]1Legacy NDC, 1 package rows20120427_d0ce87b8-d484-4307-95a9-05705a6caf85.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
65197-201-04ML - Milliliter65197-201b1293a07-b4b0-476e-b7a8-3d04c2fcad7912012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN1
SUCROSEACTIVE INGREDIENTC151H8M5541
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN1
SUCROSEACTIVE MOIETYC151H8M5541
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOA1
GLYCERININACTIVE INGREDIENTPDC6A3C0OX1
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9T1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68788-980168788-9801-1
65197-201

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554ACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
FD&C RED NO. 40WZB9127XOAIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
METHYLPARABENA2I8C7HI9TIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
METHYLPARABENMETHYLPARABENA2I8C7HI9TSOLUTION / ORAL346 mgExact identifier — unii+route+dosage form
FD&C RED NO. 40FD&C RED NO. 40WZB9127XOASOLUTION / ORAL38 mgExact identifier — unii+route+dosage form
GLYCERINGLYCERINPDC6A3C0OXSOLUTION / ORAL32400 mgExact identifier — unii+route+dosage form

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Emetrol CherryPHOSPHORATED CARBOHYDRATEWellSpring Pharmaceutical Corporationa8469128-592a-4682-82c7-4d2a6f97a9982025-06-10WarningsExact identifier
ndc (product): 65197-201
d0ce87b8-d484-4307-95a9-05705a6caf85d0ce87b8-d484-4307-95a9-05705a6caf852012-04-23WarningsExact identifier
spl id: d0ce87b8-d484-4307-95a9-05705a6caf85
spl set id: d0ce87b8-d484-4307-95a9-05705a6caf85

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.