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anti nausea

Rite Aid Corporation

Rite Aid Corporation Anti-Nausea Liquid Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients (per 5 mL)

Dextrose (glucose) 1.87 g

Levulose (fructose) 1.87 g

Phosphoric acid 21.5 mg

Purpose

Upset stomach reliever

anti nausea Uses

  • •relieves nausea due to upset stomach from intestinal flu, stomach flu, and food or drink indiscretions

Warnings

  • •this product contains fructose and should not be taken by persons with hereditary fructose intolerance (HFI)

Do not use if you have

  • •allergic reactions to any of the ingredients in this product

Ask a doctor before use if you have

  • •diabetes

Stop use and ask a doctor if

  • •symptoms persist, return or get worse

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. (1-800-222-1222)

Directions

  • •for maximum effectiveness never dilute or drink fluids of any kind immediately before or after taking this product
  • •adults and children 12 years of age and over: one or two tablespoons
  • •children 2 to under 12: one or two teaspoons
  • •repeat dose every 15 minutes or until distress subsides
  • •do not take more than 5 doses in 1 hour without consulting a doctor.

anti nausea Other information

  • •store at 20°-25°C (68°-77°F)

Inactive ingredients

FD&C red no. 40 aluminum lake, flavor, glycerin, methylparaben, purified water

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

Compare to the active ingredients of Emetrol®

anti-nausea liquid

dextrose (glucose) 1.87 g

levulose (fructose) 1.87 g

phosphoric acid 21.5 mg

for children and adults

relief for nausea due to upset stomach

cherry flavor

4 FL OZ (118 mL)

anti nausea

Dextrose (glucose), Levulose (fructose), Phosphoric Acid LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11822-0207
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DEXTROSE 1.87 g
FRUCTOSE FRUCTOSE 1.87 g
phosphoric acid PHOSPHORIC ACID 21.5 mg

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
METHYLPARABEN
water

Product Characteristics

Color
RED (clear)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 118 in 1 BOTTLE
2 NDC:11822-0207-4 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1996-06-12


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Be sure to consult your doctor before taking any medication!
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