- Active ingredients (per 5 mL)
- Purpose
- Uses
- Warnings
-
Directions
- •
- for maximum effectiveness, never dilute or drink fluids of any kind immediately before or after taking this product
- •
- repeat dose every 15 minutes or until distress subsides
- •
- do not take more than 5 doses in 1 hour without consulting a doctor
- •
- measure only with dosing cup provided. Dosing cup to be used with this product only. Do not use with other products.
- •
- mL = milliliters
age
dose
adults and children 12 years of age and over
15 mL or 30 mL
children 2 to under 12 years of age
5 mL or 10 mL
- Other information
- Inactive ingredients
- Questions or comments?
- Package/Label Principal Display Panel
-
INGREDIENTS AND APPEARANCE
FORMULA EM
dextrose (glucose), levulose (fructose), phosphoric acid solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-0049 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROSE (UNII: IY9XDZ35W2) (DEXTROSE - UNII:IY9XDZ35W2) DEXTROSE 1.87 g in 5 mL FRUCTOSE (UNII: 6YSS42VSEV) (FRUCTOSE - UNII:6YSS42VSEV) FRUCTOSE 1.87 g in 5 mL PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 21.5 mg in 5 mL Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) WATER (UNII: 059QF0KO0R) Product Characteristics Color RED (clear) Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0904-0049-20 1 in 1 CARTON 04/15/1994 1 118 mL 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 04/15/1994 Labeler - Major Pharmaceuticals (191427277)