Label: WALGREENS UPSET STOMACH AND NAUSEA RELIEF- sodium citrate dihydrate tablet, chewable
- NDC Code(s): 0363-1834-42
- Packager: WALGREENS CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 15, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
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Directions
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- Adults: 2-4 tablets.
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- Children: Consult a doctor for appropriate dosage.
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- Chew tablets completely. Do not swallow whole
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- Dosage may be repeated after 15 minutes, not to exceed 24 tablets in a 24-hour period unless advised by a doctor.
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- Read all package directions and warnings before use and use only as directed.
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- These tablets are intended for use by normally healthy persons only.
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- Persons under 18 years of age should use only as directed by a doctor.
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Other information
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- Each table contains: Sodium 60mg
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- Store at room temperature
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- Protect product from excessive heat, cold and moisture
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- Note: This product is not intended as a substitute for a balanced nutritional diet or as an electrolyte replenishment.
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- You may report serious side effects to the phone number provided under Questions.
- Inactive ingredients
- Questions or Comments?
- Distributed By
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PACKAGE LABEL
Compare to the active ingredient in Emetrol®Tablets*
NDC 0363-1834-42
Upset Stomach & Nausea Relief Tablets
For upset stomach & Nausea
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- Aspirin Free
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- Salicylate-free
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- No Gluten
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- No Aspartame
Natural Lemon Flavor
42 Chewable Tablets
IMPORTANT: Keep this carton for future reference for full labeling.
TAMPER EVIDENT: DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING.
*This product is not manufactured or distributed by WellSpring Pharmaceuticals Corporation, owner of the registered trademark Emetrol®Tablets.
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INGREDIENTS AND APPEARANCE
WALGREENS UPSET STOMACH AND NAUSEA RELIEF
sodium citrate dihydrate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-1834 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 230 mg Inactive Ingredients Ingredient Name Strength DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) LEMON (UNII: 24RS0A988O) FRUCTOSE (UNII: 6YSS42VSEV) HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color WHITE (White) Score no score Shape ROUND Size 16mm Flavor LEMON Imprint Code RP183 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-1834-42 1 in 1 BOX 12/29/2025 1 42 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 12/29/2025 Labeler - WALGREENS CO. (008965063)
