NAUZENE- sodium citrate syrup

Nauzene by

Drug Labeling and Warnings

Nauzene by is a Otc medication manufactured, distributed, or labeled by Alva-Amco Pharmacal Companies, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients (in each 15-mL tablespoon)

Dextrose (glucose) 4.35 g...........................anti-nausea

Levulose (fructose) 4.17 g...........................anti-nausea

Sodium citrate dihydrate, 0.921 g................antacid

Uses

For the relief of nausea associated with upset stomach, including that due to overindulgence in food or drink.

Warnings

DO NOT USE

Do not use if you have Hereditary Fructose Intolerance (HFI).  This product contains fructose.

Ask a doctor before use if you

• you have diabetes because this product contains sugar
• are on a sodium-restricted diet.
  

ASK DOCTOR/PHARMACIST

Ask a doctor or pharmacist before use if you are taking any other medications.  Antacids may interact with certain prescription drugs.

WHEN USING

When using this product do not take more than 6 does in a 24-hour period.

STOP USE

Stop use and ask a doctor if nausea lasts more than two weeks or recurs frequently.

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

• Read all package directions and warnings before use and use only as directed.
• Adults:  1 - 2 tablespoons (15 - 30 mL).
• Children:  Consult a doctor for appropriate dosage.
• Dosage may be repeated after 30 minutes not to exceed 6 doses in a 24-hour period unless advised by a doctor.
• For maximum effectiveness never dilute Nauzene or drink fluids of any kind immediately before or after taking Nauzene.
• Nauzene Liquid is intended for use by normally healthy persons only.
• Persons under 18 years of age should use only as directed by a doctor.
  

Other information

• Sodium content 193 mg/tablespoon (15 mL).
• Store at room temperature.
• ** Contents sealed:  Each bottle of Nauzene Liquid has a tamper evident seal around the cap and a safety seal under the cap.  Do not use if either of these seals appears broken.  NOTE:  Nauzene is not intended as a substitute for a balanced nutritional diet or as an electrolyte replenishment.
• Serious side effects associated with the use of this product may be reported to the phone number provided below.
  

Inactive ingredients

Corn syrup, FDC Red No. 40 lake, flavor, fructose syrup, glycerin, methylparaben, phosphoric acid, purified water.

QUESTIONS

Questions? 1-800-792-2582

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NAUZENE 
sodium citrate syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52389-172
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL)	TRISODIUM CITRATE DIHYDRATE	.921 g  in 15 mL
Dextrose (UNII: IY9XDZ35W2) (Dextrose - UNII:IY9XDZ35W2)	Dextrose	4.35 g  in 15 mL
Fructose (UNII: 6YSS42VSEV) (Fructose - UNII:6YSS42VSEV)	Fructose	4.17 g  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
corn syrup (UNII: 9G5L16BK6N)
FD&C Red No. 40 (UNII: WZB9127XOA)
High fructose corn syrup (UNII: XY6UN3QB6S)
Glycerin (UNII: PDC6A3C0OX)
Methylparaben (UNII: A2I8C7HI9T)
Phosphoric acid (UNII: E4GA8884NN)
Water (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY (flavor)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52389-172-04	118 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part357	02/15/2000

Labeler - Alva-Amco Pharmacal Companies, Inc. (042074856)