FDA.reportPublic FDA data

WALGREEN

Manufacturer
WALGREENS CO.
Effective date
2026-01-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:33:28

Label at a glance#

ProductWALGREEN CHILDREN ANTI NAUSEA
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= milliliter   age   dose children under 2 years ...

Label contents#

Full prescribing information#

Active ingredients (per 5ml)

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 the child has

OTC - DO NOT USE SECTION

  • allergic reactions to any of the ingredients in this product

Ask a doctor before use if the child has

OTC - ASK DOCTOR SECTION

  • diabetes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • symptoms persist, return or get worse

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
  • age
  • dose

children under 2 years

Do not use

children 2 to under 12 years of age

5 mL or 10mL

children 12 years of age and over

15 mL or 30 mL

Other information

OTHER SAFETY INFORMATION

  • Store at room temperature, away from heat and direct light; keep from freezing

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions or Comments?

OTC - QUESTIONS SECTION

1-866-467-2748

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to the active ingredients in Children’s Emetrol®*

NDC 0363-7081-04

Children Anti-Nausea Liquid

Relief from nausea due to upset stomach

Safe and effective for children

  • No antihistamines
  • No salicylates
  • No caffeine

Berry Flavor

Naturally and Artificially Flavored

4 FL. OZ. (118 mL)

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

TAMPER EVIDENT: DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING

Distributed by

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

WAG Children Anti-nausea Liquid 4 FL OZ.
WAG Children Anti-nausea Liquid 4 FL 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 SolutionPSN1
318146fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral SolutionSCD1
318146dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG per 5 ML Oral SolutionSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130000000000000GTIN-13: 0000000000000
EAN-13: 0000000000000
GTIN-12: 000000000000
UPC-A: 000000000000
GTIN storage (14 digits): 00000000000000		emetrol-childrens-mixed-berry-4oz-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
0363-7081-04WALGREENCHILDREN ANTI NAUSEA118 mL in 1 BOTTLESOLUTION1181
0363-7081-04WALGREENCHILDREN ANTI NAUSEA1 in 1 CARTONSOLUTION11

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
0363-70810363-7081-04

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
WALGREEN CHILDREN ANTI NAUSEADEXTROSE, LEVULOSE, PHOSPHORIC ACIDWALGREENS CO.1c5659ec-100f-49c6-8f2c-58c14fc7dfed2026-01-16WarningsExact identifier
ndc (package): 0363-7081-04
ndc (product): 0363-7081
ndc11 (package): 00363708104
spl id: 1c5659ec-100f-49c6-8f2c-58c14fc7dfed
spl set id: 1c5659ec-100f-49c6-8f2c-58c14fc7dfed

Reported adverse events (FAERS/openFDA)#

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