Anti Nausea Liquid

Manufacturer
TOPCO ASSOCIATES LLC
Effective date
2025-11-10
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:43:14

Label at a glance#

ProductAnti Nausea Liquid
Active ingredientDEXTROSE, UNSPECIFIED FORM, FRUCTOSE, PHOSPHORIC ACID
Label structure10 sections

Indications and uses

For relief of upset stomach associated with nausea.

Dosage and administration

for maximum effectiveness never dilute or drink fluids of any kind immediately before or after taking this product 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 this product only. Do not use with other products. mL= milliliter age dose adults and children 12 years of age a...

Label contents#

Full prescribing information#

Active ingredients (per 5 mL)

OTC - ACTIVE INGREDIENT SECTION

Dextrose (glucose) 1.87 g

Levulose (fructose) 1.87 g

  • Phosphoric acid 21.5 mg

Purpose

OTC - PURPOSE SECTION

Upset Stomach Reliever       

Uses

INDICATIONS & USAGE SECTION

For relief of upset stomach associated with nausea.

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
  • 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 this product only. Do not use with other products.
  • mL= milliliter
  1. age
  1. dose
  1. adults and children 12 years of age and over
  1. 15 mL or 30 mL
  1. children 2 to under 12 years of age
  1. 5 ml or 10 mL

Other information

SPL UNCLASSIFIED SECTION

  • Store at room temperature away from heat and direct light; keep from freezing
  • Do not use if printed seal under cap is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions or Comments?

SPL UNCLASSIFIED SECTION

1-888-423-0139

SPL UNCLASSIFIED SECTION

TopCare ®health™

Compare to Emetrol ®Active Ingredients*

Anti - Nausea Liquid

Relief from Nausea due to Upset Stomach

Safe and Effective for Children and Adults

FREE FROM:

  • Antihistamines
  • Salicylates
  • Alcohol
  • Caffeine

CHERRY FLAVOR

Naturally and Artificially Flavored

IMPORTANT :Keep this carton for future reference on full labeling.

DISTRIBUTED BY TOPCO ASSOCIATES LLC

ELK GROVE VILLAGE IL 60007

©TOPCO RARA0318

QUESTIONS? 1-888-423-0139

topcare@topco.comwww.topcarebrand.com

This TopCare ®product is laboratory tested to guarantee its highest quality.

Your total satisfaction is guaranteed.

This product is not manufactured or distributed by Wellspring Pharmaceutical Corporation., owner of the registered trademark Emetrol ®.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TopCare health Anti-Nausea LiquidTopCare health Anti-Nausea Liquid 

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 SolutionPSN8
318146fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral SolutionSCD8
318146dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG per 5 ML Oral SolutionSY8

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130036800334397GTIN-13: 0036800334397
EAN-13: 0036800334397
GTIN-12: 036800334397
UPC-A: 036800334397
GTIN storage (14 digits): 00036800334397
emetrol-1.jpg

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36800-708-04Anti Nausea Liquid118 mL in 1 BOTTLESOLUTION1188
36800-708-04Anti Nausea Liquid1 in 1 CARTONSOLUTION18

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
36800-70836800-708-04

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72024-11-06full-release2026-06-01 00:34:36

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
Anti Nausea LiquidPHOSPHORATED CARBOHYDRATETOPCO ASSOCIATES LLCfd0e8feb-89b5-42ff-806a-55b7473cf5872025-11-10WarningsExact identifier
ndc (package): 36800-708-04
ndc (product): 36800-708
ndc11 (package): 36800070804
spl id: 433baaad-076b-9bc3-e063-6394a90a26f0
spl set id: fd0e8feb-89b5-42ff-806a-55b7473cf587

Reported adverse events (FAERS/openFDA)#

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