Indications and uses
For the relief of nausea associated with upset stomach, including that due to overindulgence in food and drink.
Emetrol Powder
- Manufacturer
- WellSpring Pharmaceutical Corporation
- Effective date
- 2025-01-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 00:51:31
Label at a glance#
ProductEmetrol Powder Non-Drowsy
Active ingredientTRISODIUM CITRATE DIHYDRATE
Label structure10 sections
Dosage and administration
Adults: 1-2 packets 3 to 4 times a day. Children: Consult a doctor for appropriate dosage. Dosage may be repeated after 15 minutes, not to exceed 4 packets in a 24-hour period unless advised by a doctor. Dissolve contents of one (1) packet in 4 oz. of room temperature water before consumption. Stir again if needed Read all package directions and warnings before use and use only as directed.
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredients (in each packet)
- Sodium citrate dihydrate USP 460 mg
Purpose
Upset stomach reliever
Uses
For the relief of nausea associated with upset stomach, including that due to overindulgence in food and drink.
Warnings
Ask a doctor before use if you
- have diabetes because this product contains sugar
- are on a sodium-restricted diet
Ask a doctor or pharmacist before use if
- you are taking any other medications. This product may interact with certain prescription drugs.
When using this product,
- do not take more than 4 packets in a 24-hour period.
Stop use and ask a doctor if
- nausea lasts more than two weeks or recurs frequently.
If pregnant or breast-feeding,
- ask a health professional before use.
Keep out of reach of children
In case of overdose, get medical help or contact a Poison Control Center right away.
Directions
- Adults: 1-2 packets 3 to 4 times a day.
- Children: Consult a doctor for appropriate dosage.
- Dosage may be repeated after 15 minutes, not to exceed 4 packets in a 24-hour period unless advised by a doctor.
- Dissolve contents of one (1) packet in 4 oz. of room temperature water before consumption. Stir again if needed
- Read all package directions and warnings before use and use only as directed.
Other information
- Each table contains: Sodium 110 mg/8 g
- Store at room temperature
- Protect product from excessive heat, cold and moisture.
- Note: This product is not intended as a substitute for a balanced nutritional diet or as an electrolyte replenishment.
Inactive ingredients
Citric acid anhydrous, natural & artificial lemon flavor, silica, sucralose, sucrose.
Questions or Comments?
1-844-241-5454 or Emetrol.com
Distributed By
WellSpring Pharmaceutical Corporation
Sarasota, FL 34243
(c) 2023 WellSpring Pharmaceutical Corporation
PACKAGE LABEL
PHARMACIST RECOMMENDED
NDC# 65197-203-09
New
Non-Drowsy
Emetrol POWDER
Rapid Nausea Relief
- Treats the source of Nausea*
- Dissolve Faster in your Stomach
- Great Tasting Lemon Flavor
- Specially Formulated for Adults
*Due to overindulgence in food and drink
FSA/HAS Eligible
lemon flavor
6 PACKAETS
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 2671579 | Emetrol Powder 460 MG Powder for Oral Solution | PSN | 3 |
| 2671573 | sodium citrate 460 MG Powder for Oral Solution | PSN | 3 |
| 2671579 | sodium citrate 460 MG Powder for Oral Solution [Emetrol Powder] | SBD | 3 |
| 2671573 | sodium citrate 460 MG Powder for Oral Solution | SCD | 3 |
| 2671579 | Emetrol Powder 460 MG Powder for Oral Solution | SY | 3 |
| 2671573 | sodium citrate 460 MG Powder for Oral Solution | SY | 3 |
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| ANHYDROUS CITRIC ACID Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 65197-203-09 | Emetrol PowderNon-Drowsy | 6 in 1 CARTON | POWDER, FOR SOLUTION | 6 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Emetrol Powder Non-Drowsy
- Sodium Citrate Dihydrate
- TRISODIUM CITRATE DIHYDRATE
- ANHYDROUS CITRIC ACID
- LEMON
- SILICON DIOXIDE
- SUCRALOSE
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 65197-203 | 65197-203-09 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| TRISODIUM CITRATE DIHYDRATE | B22547B95K | ACTIM |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| LEMON | 24RS0A988O | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| SUCROSE | C151H8M554 | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Emetrol Powder Non-Drowsy | SODIUM CITRATE DIHYDRATE | WellSpring Pharmaceutical Corporation | 9d8d2ee7-9db7-4be7-8c73-511eb2e32459 | 2025-01-08 | Warnings | 65197-203-09 65197-203 65197020309 a6121b17-e850-4677-9ad1-ceb36de16336 9d8d2ee7-9db7-4be7-8c73-511eb2e32459 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.