You are here: Home > Over-the-counter (OTC) Drugs > B > Banophen (Nash-finch Company)

Name:Banophen
Manufacturer:Nash-finch Company
Category:Over-the-counter (OTC) Marketed Drugs


Our Family 44-190

BANOPHEN - diphenhydramine hydrochloride capsule 
NASH-FINCH COMPANY

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Our Family 44-190

Active ingredient (in each banded capsule)

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • runny nose

  • itchy, watery eyes

  • sneezing 

  • itching of the nose or throat

  • 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

  • a breathing problem such as emphysema or chronic bronchitis

  • glaucoma

  • 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 of 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 to 6 hours

  • do not take more than 6 doses in 24 hours
    adults and children 12 years of age and over 1 to 2 capsules 
    children 6 to under 12 years of age 1 capsule 
    children under 6 years of age do not use this product in children under 6 years of age 

Other information

  • store at controlled room temperature 15°-30°C (59°-86°F)

  • protect from moisture

  • see end flap for expiration date and lot number

Inactive ingredients

butylparaben, corn starch, D&C red #28, edible ink, FD&C blue #1, FD&C red #40, gelatin, lactose, magnesium stearate, methylparaben, propylparaben, polysorbate 80, silica gel

Questions or comments?

1-800-426-9391

Principal Display Panel

The product packaging shown below represents a sample of that currently in use. Additional packaging may also be available.

SAFETY SEALED

Allergy Relief

Compare to the Active Ingredient of Benadryl®*

Our Family®

Quality Care Since 1904

ALLERGY

COMPELTE RELIEF

Diphenhydramine HCl 25 mg

Antihistamine

Relieves: Sneezing • Itchy, Watery Eyes • Runny Nose • Itchy Throat

EASY TO SWALLOW CAPSULE

24 CAPSULES

Each capsule individually banded for your protection

TAMPER EVIDENT: PRODUCT SEALED IN PLASTIC STRIPS, CAPSULE BANDED FOR YOUR PROTECTION.  DO NOT USE IF BLISTER UNIT IS TORN OR BROKEN OR IF RED BAND AROUND CAPSULE IS BROKEN OR MISSING

DISTRIBUTED BY

NASH FINCH COMPANY ©2004, 1996

NFC BRANDS

7600 FRANCE AVE S, MPLS, MN 55435

www.ourfamilyfoods.com    NF13976

50844    REV0810C19008

Allergy Complete


BANOPHEN 
diphenhydramine hcl capsule
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:70253-190
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg
Inactive Ingredients
Ingredient Name Strength
BUTYLPARABEN  
D&C RED NO. 28  
FD&C BLUE NO. 1  
D&C RED NO. 28  
GELATIN  
LACTOSE  
MAGNESIUM STEARATE  
METHYLPARABEN  
PROPYLPARABEN  
POLYSORBATE 80  
Product Characteristics
Color PINK Score no score
Shape CAPSULE Size 14mm
Flavor Imprint Code 44;190
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70253-190-08 1 BOTTLE, PLASTIC (1 BOTTLE) in 1 CARTON contains a BOTTLE, PLASTIC
1 24 CAPSULE (24 CAPSULE) in 1 BOTTLE, PLASTIC This package is contained within the CARTON (70253-190-08)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part336 03/15/1990

Labeler - NASH-FINCH COMPANY (006962294)

Revised: 04/2011 NASH-FINCH COMPANY



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


Copyright © 2019 Drugsdb.eu by Dionisios Fentas || Terms of Use

Loading

OTC Marketed Drugs Alphabetically
A| B| C| D| E| F| G| H| I| J| K| L| M| N| O| P| Q| R| S| T| U| V| W| X| Y| Z| 0-9

Categories:
Prescription(RX) Drugs
Over-the-counter (OTC) Drugs
Homeopathic Drugs
Animal Drugs
Feedback