Active Ingredients (In Each Packet)
Sodium citrate dihydrate USP 460 mg
The following Structured Product Label (SPL) was submitted to the FDA by Wellspring Pharmaceutical Corporation for the product Emetrol Powder (NDC 65197-203). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients (in each packet), purpose, uses, ask a doctor before use if you, ask a doctor or pharmacist before use if, when using this product,, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Upset stomach reliever
For the relief of nausea associated with upset stomach, including that due to overindulgence in food and drink.
In case of overdose, get medical help or contact a Poison Control Center right away.
Citric acid anhydrous, natural & artificial lemon flavor, silica, sucralose, sucrose.
1-844-241-5454 or Emetrol.com
WellSpring Pharmaceutical Corporation
Sarasota, FL 34243
(c) 2023 WellSpring Pharmaceutical Corporation
PHARMACIST RECOMMENDED
NDC# 65197-203-09
New
Non-Drowsy
Emetrol POWDER
Rapid Nausea Relief
*Due to overindulgence in food and drink
FSA/HAS Eligible
lemon flavor
6 PACKAETS
* Please review the disclaimer below.