Label: EMETROL POWDER NON-DROWSY- sodium citrate dihydrate powder, for solution
- NDC Code(s): 65197-203-09
- Packager: WellSpring Pharmaceutical Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 13, 2024
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- Official Label (Printer Friendly)
- Active ingredients (in each packet)
- Purpose
- Uses
- Warnings
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Directions
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- Adults: 1-2 packets 3 to 4 times a day.
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- Children: Consult a doctor for appropriate dosage.
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- Dosage may be repeated after 15 minutes, not to exceed 4 packets in a 24-hour period unless advised by a doctor.
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- Dissolve contents of one (1) packet in 4 oz. of room temperature water before consumption. Stir again if needed
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- Read all package directions and warnings before use and use only as directed.
- Other information
- Inactive ingredients
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PACKAGE LABEL
PHARMACIST RECOMMENDED
NDC# 65197-203-09
New
Non-Drowsy
Emetrol POWDER
Rapid Nausea Relief
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- Treats the source of Nausea*
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- Dissolve Faster in your Stomach
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- Great Tasting Lemon Flavor
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- Specially Formulated for Adults
*Due to overindulgence in food and drink
FSA/HAS Eligible
lemon flavor
6 PACKAETS
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INGREDIENTS AND APPEARANCE
EMETROL POWDER NON-DROWSY
sodium citrate dihydrate powder, for solutionProduct 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)