FDA.reportPublic FDA data

Nausea Relief

Manufacturer
Walgreen Company
Effective date
2024-11-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 20:48:32

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

1-800-719-9260

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens

WALGREENS PHARMACIST RECOMMENDED

Compare to the active ingredients in Emetrol®

Nausea Relief

RELIEF OF NAUSEA DUE TO UPSET STOMACH

Liquid

● Safe for children & adults

● Antihistamine free

● Aspirin free

● Alcohol free

● Caffeine free

4 FL OZ (118 mL)

Cherry flavor

Nausea Relief Carton
Nausea Relief Carton

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
0363-00560363-0056-26

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

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
b41d6950-1a35-4bf6-b533-9cae25678359a62c69e4-e258-4c17-9cc3-e91848c809912024-11-27WarningsExact identifier
spl id: b41d6950-1a35-4bf6-b533-9cae25678359
spl set id: a62c69e4-e258-4c17-9cc3-e91848c80991

Reported adverse events (FAERS/openFDA)#

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