EMETROL POWDER NON-DROWSY- sodium citrate dihydrate powder, for solution

Emetrol Powder by

Drug Labeling and Warnings

Emetrol Powder by is a Otc medication manufactured, distributed, or labeled by WellSpring Pharmaceutical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

EMETROL POWDER  NON-DROWSY
sodium citrate dihydrate powder, for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65197-203
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL)	ANHYDROUS CITRIC ACID	460 mg

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
LEMON (UNII: 24RS0A988O)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	white	Score	no score
Shape		Size
Flavor	LEMON	Imprint Code	None
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65197-203-09	6 in 1 CARTON; Type 0: Not a Combination Product	12/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/01/2023

Labeler - WellSpring Pharmaceutical Corporation (110999054)