MECLIZINE HCL- meclizine hydrochloride chewable tablet, chewable 
Drug Ocean LLC

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MECLIZINE HYDROCHLORIDE CHEWABLE TABLETS 25 MG

DRUG FACTS

Active Ingredients (in each chewable tablet)

Meclizine HCl, USP 25 mg

Purpose

Antiemetic

Uses

prevents and treats nausea, vomiting or dizziness due to motion sickness.

Warnings

Do not use in children under 12 years of age unless directed by a doctor

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.

When using this product

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact the poison control center immediately

Directions

Other information

Inactive ingredients

aspartame, colloidal silicon dioxide, croscarmellose sodium, dextrose, lake of FD & C Red 40, magnesium stearate, maltodextrin, microcrystalline cellulose, raspberry flavor, sodium sulfate anhydrous, sucrose, tribasic calcium phosphate

Questions or Comments?

Call 1-844-200-6566 Monday to Friday 9 AM to 5 PM EST

TAMPER EVIDENT: DO NOT USE IF FOIL SEAL UNDER CAP, PRINTED WITH “SEALED for YOUR PROTECTION” IS BROKEN OR MISSING

Distributed by:
Drug Ocean Logo
Drug Ocean LLC,
1 Bridge Plaza, North Central Road

6th Floor, Suite 675

Fort Lee, NJ 07024

Manufactured by:

Unique Pharmaceutical Laboratories
(A Div. of J. B. Chemicals & Pharmaceuticals Ltd.)
Mumbai 400 030, India

ORG 12/23

PRINCIPAL DISPLAY PANEL - 25 mg Chewable Tablet Label

NDC 70985-010-01
Meclizine Hydrochloride Chewable Tablets 25mg
(ANTIEMETIC)
Travel Sickness
100 tablets

25 mg-100 count

MECLIZINE HCL 
meclizine hydrochloride chewable tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70985-010
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) MECLIZINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
ASPARTAME (UNII: Z0H242BBR1)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
DEXTROSE (UNII: IY9XDZ35W2)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
RASPBERRY (UNII: 4N14V5R27W)  
SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
Product Characteristics
Colorpink (Pink to light pink) Score2 pieces
ShapeROUNDSize8mm
FlavorRASPBERRYImprint Code M
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70985-010-01100 in 1 BOTTLE; Type 0: Not a Combination Product02/28/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00902/28/2022
Labeler - Drug Ocean LLC (080381835)
Registrant - Unique Pharmaceutical Laboratories (917165052)
Establishment
NameAddressID/FEIBusiness Operations
Unique Pharmaceutical Laboratories650434645manufacture(70985-010)

Revised: 12/2023
Document Id: 0d305bb7-f894-4b45-e063-6294a90ad8ed
Set id: eebd2801-62a7-471d-8e39-ac9677864aa5
Version: 6
Effective Time: 20231223
 
Drug Ocean LLC