nausea relief

Manufacturer
Kroger Company
Effective date
2023-02-02
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:38:23

Label at a glance#

Productnausea relief
Active ingredientDEXTROSE, UNSPECIFIED FORM, FRUCTOSE, PHOSPHORIC ACID
Label structure9 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 = milliliters age dose adults and children 12 y...

Storage and handling

• store at 20-25 ° C (68-77 ° F) away from heat and direct light; keep from freezing. • do not use if printed neckband is broken or missing

Label contents#

Full prescribing information#

Active ingredients (per 5 mL)

OTC - ACTIVE INGREDIENT SECTION

Dextrose (glucose) 1.87g

Levulose (fructose) 1.87g

Phosphoric acid 21.5mg

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

OTC - DO NOT USE SECTION

if you have

  • 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 = milliliters

age

dose

adults and children 12 years of age and over

15 mL or 30 mL

children 2 to under 12 years of age

5 mL or 10 mL

Other information

STORAGE AND HANDLING SECTION

  • store at 20-25°C (68-77°F) away from heat and direct light; keep from freezing.
  • do not use if printed neckband is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

FD&C red no. 40 aluminum lake, flavor, glycerin, methylparaben, purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-632-6900

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COMPARE TO the active ingredients of EMETROL® See side panel

OUR PHARMACIST RECOMMENDED

Nausea Relief

For Nausea Due to Upset Stomach

For Children & Adults

No Antihistamines

No Aspirin

No Alcohol

No Caffeine

Cherry Flavor

4 FL OZ (118 mL)

nausea relief image
nausea relief image

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30142-70930142-709-26

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

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
d19e16c7-9baa-46b6-a8c0-0b8ab17b20b35a68bf43-4035-4bed-bb94-18a6314bb2672023-02-02WarningsExact identifier
spl id: d19e16c7-9baa-46b6-a8c0-0b8ab17b20b3
spl set id: 5a68bf43-4035-4bed-bb94-18a6314bb267

Reported adverse events (FAERS/openFDA)#

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