BANOPHEN- diphenhydramine hcl capsule

Banophen by

Drug Labeling and Warnings

Banophen by is a Otc medication manufactured, distributed, or labeled by Bryant Ranch Prepack. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (in each banded capsule)

Diphenhydramine Hydrochloride 50 mg

Purpose

Antihistamine

Use

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies

• runny nose
• sneezing
• itchy, watery eyes
• itchy throat and nose
• Temporarily relieves these symptoms due to the common cold
  • runny nose
  • sneezing

WARNINGS

Do not use

• to make a child sleepy
• with any other product containing diphenhydramine, even one used on skin

Ask a doctor before use if you have

• 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 you are taking sedatives or tranquilizers

When using this product

• marked drowsiness may occur
• avoid alcoholic drinks
• alcohol, sedatives, and tranquilizers may increase drowsiness
• be careful when driving a motor vehicle or operating machinery
• excitability may occur, especially in children

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

• Take every 4-6 hours
• Do not take more than 6 doses in 24 hours

adults and children 12 years of age and over	Take 1 capsule (50 mg)
children under 12 years of age	ask a doctor, the proper dosage strength is not available in this package**
**Do not attempt to break capsules. The proper dosage strength and dosing information for children under 12 years of age is available on the 25 mg package.

Other Information

• Store at room temperature, USP.
• Do not use if either capsule band or imprinted safety seal under cap is broken or missing
• Protect from moisture
• Contains lactose

Inactive Ingredients

D&C Red #28, FD&C Blue #1, FD&C Red #40, Gelatin, Lactose and Starch.

Questions?

Questions or comments? (800) 616-2471

Distributed by

MAJOR® PHARMACEUTICALS
17177 N Laurel Park Drive, Suite 233,
Livonia, MI 48152

HOW SUPPLIED

Product: 71335-0081

NDC: 71335-0081-1 15 CAPSULE in a BOTTLE

NDC: 71335-0081-2 20 CAPSULE in a BOTTLE

NDC: 71335-0081-3 30 CAPSULE in a BOTTLE

NDC: 71335-0081-4 10 CAPSULE in a BOTTLE

NDC: 71335-0081-5 6 CAPSULE in a BOTTLE

NDC: 71335-0081-6 100 CAPSULE in a BOTTLE

NDC: 71335-0081-7 90 CAPSULE in a BOTTLE

NDC: 71335-0081-8 60 CAPSULE in a BOTTLE

NDC: 71335-0081-9 2 CAPSULE in a BOTTLE

NDC: 71335-0081-0 12 CAPSULE in a BOTTLE

Diphenhydramine 50mg Capsule

INGREDIENTS AND APPEARANCE

BANOPHEN 
diphenhydramine hcl capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71335-0081(NDC:0904-5307)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	50 mg

Inactive Ingredients
Ingredient Name	Strength
D&C RED NO. 28 (UNII: 767IP0Y5NH)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	pink	Score	no score
Shape	CAPSULE	Size	14mm
Flavor		Imprint Code	CPC;836
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71335-0081-1	15 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016
2	NDC: 71335-0081-2	20 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016
3	NDC: 71335-0081-3	30 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016
4	NDC: 71335-0081-4	10 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016
5	NDC: 71335-0081-5	6 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016
6	NDC: 71335-0081-6	100 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016
7	NDC: 71335-0081-7	90 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016
8	NDC: 71335-0081-8	60 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016
9	NDC: 71335-0081-9	2 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016
10	NDC: 71335-0081-0	12 in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	11/02/2009

Labeler - Bryant Ranch Prepack (171714327)

Establishment
Name	Address	ID/FEI	Business Operations
Bryant Ranch Prepack		171714327	REPACK(71335-0081) , RELABEL(71335-0081)