Label: MOTION SICKNESS RELIEF LESS DROWSY- meclizine hcl tablet
- NDC Code(s): 21130-778-02, 21130-778-22
- Packager: Better Living Brands, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 16, 2023
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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
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
- a breathing problem such as emphysema or chronic bronchitis
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Signature
Care®Quality
GuaranteedCOMPARE TO
Dramamine®
Less Drowsy
active ingredient*NDC 21130-778-02
Less Drowsy Formula
Motion Sickness Relief
Meclizine HCl 25 mg | AntiemeticHelps prevent Nausea, Vomiting and
Dizziness due to Motion Sickness
for up to 24 hoursAges 12 Years and Over
12 TABLETS
Actual
SizeTAMPER EVIDENT: Use Only if This Blister is Intact
*This product is not manufactured or distributed by
Medtech Products Inc., distributors of Dramamine®
Less Drowsy. 50844 ORG042340302DISTRIBUTED BY:
BETTER LIVING BRANDS LLC
P.O. BOX 99
PLEASANTON, CA 94566-0009
‡1-888-723-3929Signature Care 44-403A
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INGREDIENTS AND APPEARANCE
MOTION SICKNESS RELIEF LESS DROWSY
meclizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-778 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:21130-778-02 1 in 1 PACKAGE 06/24/2002 1 12 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:21130-778-22 4 in 1 PACKAGE 06/24/2002 09/21/2017 2 8 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 06/24/2002 Labeler - Better Living Brands, LLC (009137209) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(21130-778) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(21130-778) , pack(21130-778) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(21130-778) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(21130-778)