Anti Nausea description, usages, side effects, indications, overdosage, supplying and lots more!

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Anti Nausea

H E B

HEB Anti-Nausea 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 Emetrol® active ingredients

ANTI-NAUSEA

For Children and Adults

Relief For Nausea due to Upset Stomach

Safe for Children with Flu or Fever

Cherry Flavored

Liquid

GLUTEN FREE

Anti Nausea

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

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37808-001
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:37808-001-26 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1995-11-22


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Be sure to consult your doctor before taking any medication!
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