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Allergy Relief by Rite Aid Corporation

Dosage form: tablet, film coated
Ingredients: DIPHENHYDRAMINE HYDROCHLORIDE 25mg
Labeler: Rite Aid Corporation
NDC Code: 11822-0329

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.

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:
    • 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
  • 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 (1-800-222-1222) right away.

Directions
  • 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 yearsdo 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
  • protect from moisture
  • store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
  • see end flap for expiration date and lot number

Inactive ingredients

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

Questions or comments?

 1-800-426-9391

Principal Display Panel

RITE
AID®
PHARMACY

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

allergy relief
diphenhydramine HCl 25 mg
antihistamine

relief of:
sneezing
itchy, watery eyes
runny nose
itchy throat

easy to swallow

ACTUAL SIZE

48 MINITABS
25 mg EACH
SMALL TABLET SIZE

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

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

50844        REV1016C32922

DISTRIBUTED BY: 
RITE AID
30 HUNTER LANE
CAMP HILL, PA 17011

IF YOU'RE NOT
SATISFIED, WE'LL
HAPPILY REFUND
YOUR MONEY.

Rite Aid 44-329

ALLERGY RELIEF 
diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0329
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE 
D&C RED NO. 27 
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS 
MAGNESIUM STEARATE 
POLYETHYLENE GLYCOL, UNSPECIFIED 
SILICON DIOXIDE 
STEARIC ACID 
TITANIUM DIOXIDE 
STARCH, CORN 
TALC 
POLYVINYL ALCOHOL, UNSPECIFIED 
Product Characteristics
ColorPINKScoreno score
ShapeOVALSize11mm
FlavorImprint Code44;329
Contains    
Packaging
#Item CodePackage Description
1NDC:11822-0329-73 BLISTER PACK in 1 CARTON
112 TABLET, FILM COATED in 1 BLISTER PACK
2NDC:11822-0329-82 BLISTER PACK in 1 CARTON
212 TABLET, FILM COATED in 1 BLISTER PACK
3NDC:11822-0329-44 BLISTER PACK in 1 CARTON
312 TABLET, FILM COATED in 1 BLISTER PACK
4NDC:11822-0329-51 BLISTER PACK in 1 CARTON
412 TABLET, FILM COATED in 1 BLISTER PACK
5NDC:11822-0329-61 BOTTLE, PLASTIC in 1 CARTON
5200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
6NDC:11822-0329-31 BOTTLE, PLASTIC in 1 PACKAGE
610 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
7NDC:11822-0329-21 BOTTLE, PLASTIC in 1 CARTON
7100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
8NDC:11822-0329-1365 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34103/02/1990
Labeler - Rite Aid Corporation (014578892)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867894MANUFACTURE(11822-0329)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(11822-0329)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.868734088MANUFACTURE(11822-0329), PACK(11822-0329)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.967626305PACK(11822-0329)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867837PACK(11822-0329)

 
Rite Aid Corporation

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Medically reviewed on Apr 16, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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