Label: MOTION SICKNESS RELIEF- dimenhydrinate 50 mg tablet
- NDC Code(s): 11673-354-24
- Packager: TARGET CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 29, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- WHEN USING
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
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:
Adults and children 12 years and over
- take 1 to 2 tablets every 4-6 hours
- do not take more than 8 tablets in 24 hours, or as directed by a doctor
Children 6 to under 12 years
- give ½ to 1 tablet every 6-8 hours
- do not give more than 3 tablets in 24 hours, or as directed by a doctor
Children 2 to under 6 years
- give ½ tablet every 6-8 hours
- do not give more than 1 ½ tablets in 24 hours, or as directed by a doctor
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MOTION SICKNESS RELIEF
dimenhydrinate 50 mg tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-354 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 HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) MAGNESIUM STEARATE (UNII: 70097M6I30) MINERAL OIL (UNII: T5L8T28FGP) ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) Product Characteristics Color white Score 2 pieces Shape ROUND Size 9mm Flavor Imprint Code TCL352 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-354-24 4 in 1 CARTON 03/31/2025 1 6 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 03/31/2025 Labeler - TARGET CORPORATION (006961700) Registrant - TIME CAP LABORATORIES INC (037052099) Establishment Name Address ID/FEI Business Operations TIME CAP LABORATORIES, INC 037052099 manufacture(11673-354)

