Label: MOTION SICKNESS RELIEF- dimenhydrinate tablet
- NDC Code(s): 0363-1980-08
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 12, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
-
Warnings
Ask a doctor before use if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
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Directions
- do not take more than directed
- to prevent motion sickness, the first dose should be taken 1/2 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 1/2 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 1/2 tablet every 6-8 hours
- do not give more than 1½ tablets in 24 hours, or as directed by a doctor
- Other information
- Inactive ingredients
- Questions or comments?
- Principal display panel
-
INGREDIENTS AND APPEARANCE
MOTION SICKNESS RELIEF
dimenhydrinate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-1980 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMENHYDRINATE (UNII: JB937PER5C) (DIPHENHYDRAMINE - UNII:8GTS82S83M, 8-CHLOROTHEOPHYLLINE - UNII:GE2UA340FM) DIMENHYDRINATE 50 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score 2 pieces Shape ROUND Size 9mm Flavor Imprint Code 44;198 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-1980-08 4 in 1 CARTON 10/22/2021 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 10/22/2021 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(0363-1980) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(0363-1980) , pack(0363-1980) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(0363-1980)

