Uses
INDICATIONS AND USAGE
For the management of nausea and vomiting, and dizziness associated with motion sickness.
CONTRAINDICATIONS
Meclizine Hydrochloride is contraindicated in individuals who have shown a previous hypersensitivity to it.
MECLIZINE HYDROCHLORIDE TABLETS, USP Rx only
- Manufacturer
- Proficient Rx LP
- Effective date
- 2022-06-01
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 6
- Source
- full-release
- Hydrated at
- 2026-05-31 20:42:08
Key Label Information#
Warnings
CONTRAINDICATIONS
Meclizine Hydrochloride is contraindicated in individuals who have shown a previous hypersensitivity to it.
WARNINGS
Since drowsiness may, on occasion, occur with use of this drug, patients should be warned of this possibility and cautioned against driving a car or operating dangerous machinery. Patients should avoid alcoholic beverages while taking this drug. Due to its potential anticholinergic action, this drug should be used with caution in patients with asthma, glaucoma or enlargement of the prostate gland.
Directions And Dosage
DOSAGE AND ADMINISTRATION
Motion Sickness The initial dose of 25 to 50 mg of Meclizine HCI should be taken one hour prior to travel for protection against motion sickness. Thereafter, the dose may be repeated every 24 hours for the duration of the journey.
Other Label Information
PRINCIPAL DISPLAY PANEL
NDC 63187-996-20 Meclizine Hydrochloride Tablets, USP 25 mg 20 Tablets Rx Only Each tablet Contains 25 mg of meclizine HCl DOSAGE AND USE See accompanying prescribing information MOTION SICKNESS: 25 mg to 50 mg daily. Dispense in tight, light-resistant containers (USP). Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].
Label Images#
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| MECLIZINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| ac6963c4-31c6-325f-ee58-83a0a06597ad | Product name | 5 | 20221206 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63187-996-10 | MECLIZINE HYDROCHLORIDE | 10 in 1 BOTTLE | TABLET | 10 | 6 | |
| 63187-996-20 | MECLIZINE HYDROCHLORIDE | 20 in 1 BOTTLE | TABLET | 20 | 6 | |
| 63187-996-30 | MECLIZINE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET | 30 | 6 | |
| 63187-996-60 | MECLIZINE HYDROCHLORIDE | 60 in 1 BOTTLE | TABLET | 60 | 6 | |
| 63187-996-90 | MECLIZINE HYDROCHLORIDE | 90 in 1 BOTTLE | TABLET | 90 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63187-996-10 | EA - Each | 63187-996 | 640f5d90-6124-4eee-a812-82c7ea8ea969 | 1 | 2020-08-06 |
| 63187-996-20 | EA - Each | 63187-996 | 59b801ca-8f84-4b42-af4c-ba86273953e1 | 1 | 2018-05-09 |
| 63187-996-30 | EA - Each | 63187-996 | 3ca4f632-f975-4f06-bc58-f7af9336200d | 1 | 2019-02-13 |
| 59746-121-06 | EA - Each | 59746-121 | 426b1544-2026-4b5e-92b6-b06bf4ad8883 | 1 | 2012-07-24 |
| 59746-121-10 | EA - Each | 59746-121 | ef373495-c09a-4243-9246-5944249609e5 | 1 | 2012-07-24 |
Products#
- Meclizine Hydrocloride
- Meclizine
NDC Codes#
Ingredients#
| Name | UNII | Kind |
|---|---|---|
| Meclizine Hydrochloride | HDP7W44CIO | ACTIB |
| Silicon Dioxide | ETJ7Z6XBU4 | IACT |
| Croscarmellose Sodium | M28OL1HH48 | IACT |
| Lactose Monohydrate | EWQ57Q8I5X | IACT |
| Magnesium Stearate | 70097M6I30 | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| D&c Yellow No. 10 | 35SW5USQ3G | IACT |
| Aluminum Oxide | LMI26O6933 | IACT |
Complete SPL Sections#
DESCRIPTION
Chemically, Meclizine HCl is 1-( p -chloro-α-phenylbenzyl)-4-( m -methylbenzyl) piperazine dihydrochloride monohydrate. C 25 H 27 ClN 2 . 2HCl . H 2 O M . W . 481 . 88 Meclizine HCI Tablets, USP are available in two different strengths: 12.5 mg and 25 mg. In addition each tablet contains the following inactive ingredients: Colloidal Silicon Dioxide, Croscarmellose Sodium, Lactose Monohydrate, Magnesium Stearate, Microcrystalline Cellulose. Also, Meclizine HCI Tablets USP, 12.5 mg contains FD&C Blue #1 Aluminum Lake (11-13%) and Meclizine HCI Tablets USP, 25 mg contains D&C Yellow #10 Aluminum Lake (15-20%).
CLINICAL PHARMACOLOGY
Meclizine Hydrochloride is an antihistamine which shows marked protective activity against nebulized histamine and lethal doses of intravenously injected histamine in guinea pigs. It has a marked effect in blocking the vasodepressor response to histamine, but only a slight blocking action against acetylcholine. Its activity is relatively weak in inhibiting the spasmogenic action of histamine on isolated guinea pig ileum.
INDICATIONS AND USAGE
For the management of nausea and vomiting, and dizziness associated with motion sickness.
CONTRAINDICATIONS
Meclizine Hydrochloride is contraindicated in individuals who have shown a previous hypersensitivity to it.
WARNINGS
Since drowsiness may, on occasion, occur with use of this drug, patients should be warned of this possibility and cautioned against driving a car or operating dangerous machinery. Patients should avoid alcoholic beverages while taking this drug. Due to its potential anticholinergic action, this drug should be used with caution in patients with asthma, glaucoma or enlargement of the prostate gland.
PRECAUTIONS
PREGNANCY, Teratogenic Effects Pregnancy Category B. Reproduction studies in rats have shown cleft palates at 25-50 times the human dose. Epidemiological studies in pregnant women, however, do not indicate that medicine increases the risk of abnormalities when administered during pregnancy. Despite the animal findings, it would appear that the possibility of fetal harm is remote. Nevertheless, meclizine, or any other medication, should be used during pregnancy only if clearly necessary. Pediatric Use Clinical studies establishing safety and effectiveness in children have not been done; therefore, usage is not recommended in children under 12 years of age.
ADVERSE REACTIONS
Drowsiness, dry mouth and, on rare occasions, blurred vision have been reported.
DOSAGE AND ADMINISTRATION
Motion Sickness The initial dose of 25 to 50 mg of Meclizine HCI should be taken one hour prior to travel for protection against motion sickness. Thereafter, the dose may be repeated every 24 hours for the duration of the journey.
HOW SUPPLIED
Meclizine HCI Tablets, USP are available in the following strengths and package sizes: 25 mg (Yellow, oval-shaped, scored, debossed with TL121) Bottles of 10 NDC 63187-996-10 Bottles of 20 NDC 63187-996-20 Bottles of 30 NDC 63187-996-30 Bottles of 60 NDC 63187-996-60 Bottles of 90 NDC 63187-996-90 Store at 20-25°C (68-77°F) (See USP Controlled Room Temperature]. Manufactured By: Jubilant Cadista Pharmaceuticals Inc. Salisbury, MD 21801, USA. Repackaged by: Proficient Rx LP Thousand Oaks, CA 91320 Revised 03/11
PRINCIPAL DISPLAY PANEL
NDC 63187-996-20 Meclizine Hydrochloride Tablets, USP 25 mg 20 Tablets Rx Only Each tablet Contains 25 mg of meclizine HCl DOSAGE AND USE See accompanying prescribing information MOTION SICKNESS: 25 mg to 50 mg daily. Dispense in tight, light-resistant containers (USP). Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].