Label: MOTION SICKNESS RELIEF- dimenhydrinate 50mg tablet
- NDC Code(s): 69168-408-86
- Packager: Allegiant Health
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 12, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Use
-
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
-
Directions
- to prevent motion sickness, the first dose should be taken ½ to 1 hour before starting activity
Adults and
children 12
years and over- 1 to 2 tables every 4-6 hours
- do not exceed 8 tablets in
24 hours, or as directed by a doctor
Children 6 to
under 12 years- ½ to 1 tablet every 6-8 hours
- do not exceed 3 tablets in
24 hours, or as directed by a doctor
Children 2 to
under 6 years- ½ tablet every 6-8 hours
- do not exceed 1 ½ tablets
in 24 hours, or as directed by a doctor
- to prevent motion sickness, the first dose should be taken ½ to 1 hour before starting activity
- Other information
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MOTION SICKNESS RELIEF
dimenhydrinate 50mg tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69168-408 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMENHYDRINATE (UNII: JB937PER5C) (8-CHLOROTHEOPHYLLINE - UNII:GE2UA340FM) DIMENHYDRINATE 50 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score 2 pieces Shape ROUND Size 8mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69168-408-86 1 in 1 CARTON 01/15/2012 1 12 in 1 BLISTER PACK; 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 01/15/2012 Labeler - Allegiant Health (079501930)