BONINE FASTER-ACTING- diphenhydramine hcl tablet

BONINE by

Drug Labeling and Warnings

BONINE by is a Otc medication manufactured, distributed, or labeled by WellSpring Pharmaceutical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Diphenhydramine HCl 25 mg

Purpose

Antiemetic

Uses

for prevention and treatment of nausea, vomiting, Uses or dizziness associated with motion sickness

Warnings

Do not use

■ for children under 6 years of age unless

■ Do not use with any other product containing diphenhydramine, including one used on skin

Ask a doctor before use if you have

■ difficulty in urination due to enlargement of the prostate gland

■ glaucoma

■ difficulty in urination due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

■ marked drowsiness may occur

■ alcohol, sedatives, and tranquilizers may increase drowsiness

■ avoid alcoholic beverages

■ use caution when driving a motor vehicle or operating machinery

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 a Poison Control Center right away.

Directions

■ dosage should be taken 30 minutes before you begin motion activity.

■ adults and children 12 years and over: take 1 to 2 tablets with Water every 4 to 6 hours, not to exceed 12 tablets (300 milligrams) in 24 hours, or as directed by a doctor.

■ Children 6 to under 12 years of age: take 1 tablet with Water every 4 to 6 hours, not to exceed 6 tablets (150 milligrams) in 24 hours, or as directed by a doctor.

Other information

■ Each tablet contains: Calcium 60mg 

■ Store at 25°C (77°F); excursions permitted between 15° - 30°C (59° - 86°F)

■ protect from moisture

■ see end flap for expiration date and lot number

Inactive ingredients

Croscarmellose sodium, dibasic calcium phosphate dihydrate, FD&C blue #1, aluminum lake, magnesium stearate, microcrystalline cellulose, silicone dioxide, stearic acid

Questions?

1-844-241-5454 or www.bonine.com

SPL UNCLASSIFIED SECTION

TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN. Keep Carton for important drug facts information.

Distributed by: WellSpring
Pharmaceutical Corporation
Sarasota, FL 34243
©2023 WellSpring
Pharmaceutical Corporation

Money Back Guarantee

PRINCIPAL DISPLAY PANEL 65197-616-16

NEW

9X the Adventure**

Diphenhydramine HCl - Antiemetic 25 mg

Prevents & Treats:

Vomiting    Nausea    Dizziness  Motion Sickness

*See back panel reference

* Than Meclizine HCL 25 mg per onset of action from The U.S. National Library of Medicine (NLM)

** Results may vary

FASTER-ACTING* RELIEF

TAKE WITH WATER

Bonine Faster Acting 2.0

INGREDIENTS AND APPEARANCE

BONINE  FASTER-ACTING
diphenhydramine hcl tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65197-616
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	25 mg

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	blue	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	WS1
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65197-616-16	2 in 1 BOX	05/01/2023
1		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 final	part336	05/01/2023

Labeler - WellSpring Pharmaceutical Corporation (110999054)