Meclizine Hydrochloride - Bryant Ranch Prepack

Manufacturer: Bryant Ranch Prepack
Effective date: 2026-08-20
Label type: HUMAN OTC DRUG LABEL
Version: 104
Source: daily-update
Hydrated at: 2026-08-25 01:02:16

Label at a glance#

ProductMeclizine Hydrochloride

Active ingredientMECLIZINE HYDROCHLORIDE

Label structure11 sections

Indications and uses

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

Dosage and administration

 Dosage should be taken one hour before travel starts adults and children 12 years of age and over chew 1 to 2 tablets once daily, or as directed by a doctor children under 12 years of age do not give to children under 12 years of age unless directed by a doctor

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-800-231-4670

PhoneLabel contact(800) 616-2471

Websitewww.major-rugby.com

www.major-rugby.com

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each chewable tablet)
Meclizine HCl 25 mg

OTC - PURPOSE SECTION

Purpose

Antiemetic

Uses

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings

Do not use

OTC - DO NOT USE SECTION

for children under 12 years of age unless directed by a doctor

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

 glaucoma

 a breathing problem such as emphysema or chronic bronchitis
 trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if

OTC - ASK DOCTOR/PHARMACIST SECTION

you are taking sedatives or tranquilizers

When using this product

OTC - WHEN USING SECTION

 drowsiness may occur

 alcohol, sedatives, and tranquilizers may increase drowsiness

 avoid alcoholic drinks
 use caution when driving a motor vehicle or operating machinery

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

 Dosage should be taken one hour before travel starts

adults and children 12 years of age and over	chew 1 to 2 tablets once daily, or as directed by a doctor
children under 12 years of age	do not give to children under 12 years of age unless directed by a doctor

Other information

OTHER SAFETY INFORMATION

 Store in a dry place at 15°-30°C (59°-86°F)
 keep lid tightly closed

Inactive ingredients

INACTIVE INGREDIENT SECTION

croscarmellose sodium, crospovidone, FD&C red #40 lake, french vanilla flavor, lactose, magnesium stearate, raspberry flavor, silica, sodium saccharin, stearic acid.

Questions or comments?

OTC - QUESTIONS SECTION

1-800-231-4670

SPL UNCLASSIFIED SECTION

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

*This product is not manufactured or distributed by Wellspring Pharmaceutical Corporation, owner of the registered trademark Bonine®.

Distributed by:
RUGBY® LABORATORIES
Indianapolis, IN 46268

(800) 616-2471
www.major-rugby.com

Rev. 11/25 R-29 Re-order No. 371033

HOW SUPPLIED

How Supplied Section

Meclizine HCl 25 mg

NDC: 71335-2177-1: 30 Tablets in a BOTTLE

NDC: 71335-2177-2: 20 Tablets in a BOTTLE

NDC: 71335-2177-3: 25 Tablets in a BOTTLE

NDC: 71335-2177-4: 40 Tablets in a BOTTLE

NDC: 71335-2177-5: 60 Tablets in a BOTTLE

NDC: 71335-2177-6: 90 Tablets in a BOTTLE

NDC: 71335-2177-7: 8 Tablets in a BOTTLE

NDC: 71335-2177-8: 14 Tablets in a BOTTLE

NDC: 71335-2177-9: 10 Tablets in a BOTTLE

NDC: 71335-2177-0: 120 Tablets in a BOTTLE

Repackaged/Relabeled by:
Bryant Ranch Prepack
Burbank, CA 91504

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Meclizine 25 mg Chewable

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	Data Matrix	(01)00371335217716(21)0123456789(17)280820(10)208820	GTIN-14: 00371335217716 GTIN-12: 371335217716 UPC-A: 371335217716 EAN-13: 0371335217716 GTIN storage (14 digits): 00371335217716	lbl713352177.jpg
QR code link	QR Code	dailymed.nlm.nih.gov/dailymed/search.cfm?adv=1&query=NDC:71335-2177-1		lbl713352177.jpg
Data code	Code 128	7133521771		lbl713352177.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ac6963c4-31c6-325f-ee58-83a0a06597ad	Product name	5	20221206

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0536-1299-10	EA - Each	0536-1299	4be88e27-d239-44c2-93e3-eb1867badd82	1	2021-02-05

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

Meclizine Hydrochloride
CROSPOVIDONE
VANILLA BEAN
MAGNESIUM STEARATE
RASPBERRY
STEARIC ACID
SILICON DIOXIDE
FD&C RED NO. 40
MECLIZINE
LACTOSE MONOHYDRATE
SACCHARIN SODIUM
CROSCARMELLOSE SODIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71335-2177	71335-2177-1, 71335-2177-2, 71335-2177-3, 71335-2177-4, 71335-2177-5, 71335-2177-6, 71335-2177-7, 71335-2177-8, 71335-2177-9, 71335-2177-0
0536-1299

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CROSPOVIDONE	2S7830E561	IACT
VANILLA BEAN	Q74T35078H	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
RASPBERRY	4N14V5R27W	IACT
STEARIC ACID	4ELV7Z65AP	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
MECLIZINE HYDROCHLORIDE	HDP7W44CIO	ACTIB
LACTOSE MONOHYDRATE	EWQ57Q8I5X	IACT
SACCHARIN SODIUM	SB8ZUX40TY	IACT
CROSCARMELLOSE SODIUM	M28OL1HH48	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
103	2024-04-03	full-release	2026-06-01 00:11:16

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Bryant Ranch Prepack	cd82fca9-a8dc-4545-8e64-b67d644832e7	2026-08-20	Warnings	Exact identifier ndc (package): 71335-2177-8 ndc (package): 71335-2177-3 ndc (package): 71335-2177-6 ndc (package): 71335-2177-7 ndc (package): 71335-2177-9 ndc (package): 71335-2177-2 ndc (package): 71335-2177-1 ndc (package): 71335-2177-4 ndc (package): 71335-2177-5 ndc (package): 71335-2177-0 ndc (product): 71335-2177 ndc11 (package): 71335217709 ndc11 (package): 71335217704 ndc11 (package): 71335217700 ndc11 (package): 71335217707 ndc11 (package): 71335217705 ndc11 (package): 71335217708 ndc11 (package): 71335217703 ndc11 (package): 71335217701 ndc11 (package): 71335217706 ndc11 (package): 71335217702 spl id: d2a65736-2711-4572-879b-ea3904cfcda7 spl set id: cd82fca9-a8dc-4545-8e64-b67d644832e7
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Rugby Laboratories	b57f14a7-3852-03db-e053-2a95a90a80d6	2026-07-16	Warnings	Exact identifier ndc (product): 0536-1299

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.