FDA.reportPublic FDA data

Anti Nausea

Manufacturer
Cardinal Health
Effective date
2025-10-14
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:38:58

Label at a glance#

ProductAnti Nausea
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 at (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

1-866-467-2748

SPL UNCLASSIFIED SECTION

NDC 70000-0052-1

Compare to the active ingredients EMETROL ®*

Relief from Nausea Due to Upset Stomach Safe and Effective for Children and Adults

  • No Antihistamines
  • No Salicylates
  • No Caffeine

Natural Cherry Flavor

4 FL OZ (118 mL)

LEADER ™

Non-Drowsy

Children Adult

Nausea Relief

Dextrose(Glucose)

Levulose ( Fructose)

Phosphoric Acid

Upset Stomach Reliever

Cherry Flavor

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

Distributed by:

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

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cardinal Health Anti Nausea LiquidCardinal 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 SolutionPSN7
318146fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral SolutionSCD7
318146dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG per 5 ML Oral SolutionSY7

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
70000-0052-1Anti Nausea1 in 1 CARTONLIQUID17
70000-0052-1Anti Nausea118 mL in 1 BOTTLELIQUID1187

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70000-0052-1ML - Milliliter70000-00520df2b41e-aa95-43b9-9380-320d9841419c12021-08-05

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
70000-005270000-0052-1

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
FD&C RED NO. 40WZB9127XOAIACT
GLYCERINPDC6A3C0OXIACT
METHYLPARABENA2I8C7HI9TIACT
WATER059QF0KO0RIACT
DEXTROSE, UNSPECIFIED FORMIY9XDZ35W2ACTIB
FRUCTOSE6YSS42VSEVACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62024-11-21full-release2026-06-01 00:38:28

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 NauseaDEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACIDCardinal Healthb2f0e93f-a2e9-4970-bfb8-de30a62478132025-10-14WarningsExact identifier
ndc (package): 70000-0052-1
ndc (product): 70000-0052
ndc11 (package): 70000005201
spl id: 411c8399-28ef-c4f1-e063-6394a90a76e9
spl set id: b2f0e93f-a2e9-4970-bfb8-de30a6247813

Reported adverse events (FAERS/openFDA)#

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