FDA.reportPublic FDA data

Emetrol Cherry

Manufacturer
WellSpring Pharmaceutical Corporation
Effective date
2025-06-10
Label type
HUMAN OTC DRUG LABEL
Version
35
Source
full-release
Hydrated at
2026-06-01 01:02:47

Label at a glance#

ProductEmetrol Cherry
Active ingredientDEXTROSE, PHOSPHORIC ACID, FRUCTOSE
Label structure10 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 measure only with dosing cup provided. Dosing cup to be used wit...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Phosphorated carbohydrate solution*
    *each 5 mL contains:

  • 1.87 g Dextrose (glucose)
  • 1.87 g Levulose (fructose)
  • 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
  • measure only with dosing cup provided. Dosing cup to be used with Emetrol only. Do not use with other products.

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.

Questions or Comments?

SPL UNCLASSIFIED SECTION

call 1-844-241-5454

Distributed By

SPL UNCLASSIFIED SECTION

WellSpring Pharmaceutical Corporation
Sarasota, FL 34243 USA
(c) WellSpring 2019

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Emetrol Loquid Rapid Nausea Relief

Treats the source of Nausea & upset stomach

CT201048H
CT201048H
Emetrol 12 oz
Emetrol 12 oz

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 SolutionPSN35
809602Emetrol 1.87 GM / 1.87 GM / 21.5 MG in 5 mL Oral SolutionPSN35
809602fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral Solution [Emetrol]SBD35
318146fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral SolutionSCD35
318146dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG per 5 ML Oral SolutionSY35
809602Emetrol (dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG) per 5 ML Oral SolutionSY35
809602Emetrol (sucrose 3.74 GM / phosphoric acid 21.5 MG) per 5 ML Oral SolutionSY35

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65197-201-04Emetrol Cherry1 in 1 CARTONSOLUTION135
65197-201-04Emetrol Cherry118 mL in 1 BOTTLESOLUTION11835
65197-201-06Emetrol Cherry133 mL in 1 BOTTLESOLUTION13335
65197-201-12Emetrol Cherry354 mL in 1 BOTTLESOLUTION35435

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
DEXTROSEACTIVE INGREDIENTIY9XDZ35W224
FRUCTOSEACTIVE INGREDIENT6YSS42VSEV24
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN24
DEXTROSEACTIVE MOIETYIY9XDZ35W224
FRUCTOSEACTIVE MOIETY6YSS42VSEV24
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN24
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOA24
GLYCERININACTIVE INGREDIENTPDC6A3C0OX24
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9T24
WATERINACTIVE INGREDIENT059QF0KO0R24

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65197-20165197-201-04, 65197-201-06, 65197-201-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
DEXTROSEIY9XDZ35W2ACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
FRUCTOSE6YSS42VSEVACTIB
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 · 12 matching rows.

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

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 · 1 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 (package): 65197-201-12
ndc (package): 65197-201-04
ndc (package): 65197-201-06
ndc (product): 65197-201
ndc11 (package): 65197020112
ndc11 (package): 65197020106
ndc11 (package): 65197020104
spl id: e98d894b-049d-41b1-9681-bf3867b9d379
spl set id: a8469128-592a-4682-82c7-4d2a6f97a998

Reported adverse events (FAERS/openFDA)#

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