Label: NAUZENE CHEWABLES GINGER HONEY- sodium citrate tablet, chewable
- NDC Code(s): 52389-677-42
- Packager: Kobayashi Healthcare International, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 24, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each cheable tablet)
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use if you
- Ask a doctor or pharmacist before use if you are
- When using this product,
- Stop use and ask a doctor if
- If pregnant or breast-feeding,
- Keep out of reach of children.
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Directions
- Adults: 2-4 tablets.
- Children: Consult a doctor for appropriate dosage.
- Chew tablets completely.
- Dosage may be repeated after 15 minutes, not to exceed 16 tablets in a 24-hour period unless advised by a doctor.
- Read all package directions and warnings before use and use only as directed.
- Nauzene Chewables are intended for use by normally healthy persons only.
- Persons under 18 years of age should use only as directed by a doctor.
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Other information
- Sodium content: 60 mg/tablet
- Store at room temperature.
- **Contents Sealed: Each round tan NAUZENE chewable tablet bears the identifying mark "ALVA" and is sealed in a clear plastic blister with a foil backing. Do not use if seal appears broken or if product contents do not match product description. Slight darker speckling may occur over time. Note: NAUZENE is not intended as a substitute for a balanced nutritional diet or as an electrolyte replensihment.
- You may report serious side effects to the phone number provided under Questions? below.
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NAUZENE CHEWABLES GINGER HONEY
sodium citrate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52389-677 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 (UNII: IY9XDZ35W2) POVIDONE K30 (UNII: U725QWY32X) MALIC ACID (UNII: 817L1N4CKP) STEVIA LEAF (UNII: 6TC6NN0876) ACACIA (UNII: 5C5403N26O) HYDROXYPROPYLCELLULOSE (UNII: 9XZ8H6N6OH) SUCROSE (UNII: C151H8M554) MAGNESIUM STEARATE (UNII: 70097M6I30) SUCRALOSE (UNII: 96K6UQ3ZD4) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) FRUCTOSE (UNII: 6YSS42VSEV) STEARIC ACID (UNII: 4ELV7Z65AP) ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MALTODEXTRIN (UNII: 7CVR7L4A2D) Product Characteristics Color yellow Score no score Shape ROUND Size 16mm Flavor GINGER (Ginger-Honey flavor) Imprint Code ALVA Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52389-677-42 3 in 1 CARTON 02/17/2025 1 14 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 02/17/2025 Labeler - Kobayashi Healthcare International, Inc. (156391729) Registrant - Kobayashi America Manufacturing, LLC (079852150)

