Label: GRAVOL- dimenhydrinate syrup
- NDC Code(s): 10237-942-25
- Packager: Church & Dwight Co., Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 18, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each 5 mL)
- Purpose
- Use
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Warnings
Ask a doctor before use if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- trouble urinating due to an enlarged prostate gland
- a breathing problem such as emphysema or chronic bronchitis
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Directions
- to prevent motion sickness, the first dose should be taken ½ to 1 hour before starting activity
- to prevent or treat motion sickness, see below:
children 2 to 6 years - take 1 teaspoon (5 mL) every 4-6 hours
- do not take more than 5 teaspoons (25 mL) in 24 hours, or as directed by a doctor
children 6 to under 12 years - give 2 teaspoons (10 mL) every 6-8 hours
- do not give more than 10 teaspoons (50 mL) in 24 hours, or as directed by a doctor
- Other information
- Inactive ingredients
- Questions or comments?
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PRINCIPAL DISPLAY PANEL
OVER 70 YEARS OF
QUALITY & TRUST†
Children 2+
Prevents and Treats:
Nausea & Vomiting
Dizziness*
kids Gravol™
MOTION SICKNESS RELIEF
Dimenhydrinate 15 mg Syrup - Antiemetic
*Prevention and treatment of
nausea, vomiting and dizziness
due to motion sickness
MIXED FRUIT
FLAVOR
DYE FREE ALCOHOL FREE
2.5 FL OZ (75 mL)
Church & Dwight Co., Inc.,
Ewing, NJ 08628
Gravol is a trademark of
Church & Dwight Canada Corp.
Made in Canada
GRFC-00164-01 72022778
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INGREDIENTS AND APPEARANCE
GRAVOL
dimenhydrinate syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10237-942 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMENHYDRINATE (UNII: JB937PER5C) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIMENHYDRINATE 15 mg in 5 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SUCROSE (UNII: C151H8M554) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) POLYSORBATE 80 (UNII: 6OZP39ZG8H) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBITOL (UNII: 506T60A25R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10237-942-25 1 in 1 CARTON 03/02/2022 1 75 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 OTC MONOGRAPH DRUG M009 03/02/2022 Labeler - Church & Dwight Co., Inc. (001211952)