BANOPHEN- diphenhydramine hcl tablet, film coated 
Proficient Rx LP

----------

Rite Aid 44-329

Active ingredient (in each tablet)

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
o
runny nose
o
itchy, watery eyes
o
sneezing
o
itching of the nose or throat
temporarily relieves these symptoms due to the common cold:
o
runny nose
o
sneezing 

Warnings

Do not use

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
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
avoid alcoholic beverages
alcohol, sedatives, and tranquilizers may increase drowsiness
use caution 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

do not take more than directed
take every 4 to 6 hours, or as directed by a doctor
do not take more than 6 times in 24 hours

adults and children 12
years and over

1 to 2 tablets

children 6 to under 12
years

1 tablet

children under 6 years

do not use

Other information

each tablet contains: calcium 30 mg
TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
protect from moisture
see end flap for expiration date and lot number

Inactive ingredients

corn starch, D&C red #27 aluminum lake, dibasic calcium phosphate dihydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, silicon dioxide, stearic acid, talc, titanium dioxide

Questions or comments?

(800)-616-2471

Principal Display Panel

NDC 71205-611-20

Compare to the active ingredient in Benadryl® Allergy ULTRATAB® Tablets*

Banophen
Diphenhydramine HCl
25 mg
Antihistamine / Allergy Relief

Relieves
Sneezing,  Runny Nose,
Itchy Throat and
Itchy, Watery Eyes

Actual Size

20 Minitabs

*This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Benadryl® Allergy ULTRATAB® Tablets.
50844    REV1220M32908

Rev. 03/21   M-17   Re-order No. 250050

Distributed by:
MAJOR® PHARMACEUTICALS
17177 N Laurel Park Drive, Suite 233 Livonia, MI 48152 USA

Repackaged by:
PROFICIENT RX LP
Thousand Oaks, CA 91320

TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING

71205-611-20
BANOPHEN 
diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71205-611(NDC:0904-5551)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
STARCH, CORN (UNII: O8232NY3SJ)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorpinkScoreno score
ShapeOVALSize11mm
FlavorImprint Code 44;329
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71205-611-2020 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/11/2021
2NDC:71205-611-3030 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/11/2021
3NDC:71205-611-6060 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/11/2021
4NDC:71205-611-9090 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/11/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/02/1990
Labeler - Proficient Rx LP (079196022)
Establishment
NameAddressID/FEIBusiness Operations
Proficient Rx LP079196022REPACK(71205-611) , RELABEL(71205-611)

Revised: 12/2023
Document Id: 449c7ca6-7fd4-4728-b330-2a3e261c6693
Set id: 62934d0f-b23d-4c03-9d60-a7bad41f9b42
Version: 3
Effective Time: 20231201
 
Proficient Rx LP