Label: MOTION SICKNESS- meclizine hcl tablet
- NDC Code(s): 37808-903-12
- Packager: H E B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 11, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
- difficulty in urination due to enlargement of the prostate gland
- glaucoma
- a breathing problem such as emphysema or chronic bronchitis
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
H-E-B®
NDC 37808-903-12
Compare to
Dramamine®
Less Drowsy
active ingredient*Motion
Sickness
Meclizine HCl 25 mgAntiemetic
Helps prevent Nausea
& Dizziness due to
Motion Sickness for
up to 24 hours•For Ages 12 and Over
•24 Hours of Protection
• Less Drowsy FormulaActual
Size100 TABLETS
TAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSING*This product is not manufactured or distributed by
Medtech Products Inc., owner of the registered trademark
Dramamine® Less Drowsy.
50844 ORG042340312100%
GUARANTEE
promiseMADE WITH PRIDE AND
CARE FOR H-E-B®,
SAN ANTONIO, TX 78204HEB 44-403A
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INGREDIENTS AND APPEARANCE
MOTION SICKNESS
meclizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-903 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) MECLIZINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color yellow Score no score Shape ROUND Size 9mm Flavor Imprint Code 44;403 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-903-12 100 in 1 BOTTLE; Type 0: Not a Combination Product 06/24/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M009 06/24/2019 Labeler - H E B (007924756) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(37808-903) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(37808-903) , pack(37808-903) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(37808-903) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(37808-903)