ALLERGY RELIEF- diphenhydramine hcl tablet, film coated 
Family Dollar Services Inc

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Family Wellness 44-329 Allergy Relief

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 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 over1 to 2 tablets
children 6 to under 12  years1 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
  • store at 25ºC (77ºF); excursions permitted between 15°-30°C (59°-86°F)
  • protect from moisture
  • 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

FAMILY
Wellness™

COMPARE TO THE ACTIVE
INGREDIENT IN BENADRYL®
ALLERGY ULTRATAB® TABLETS*

ALLERGY RELIEF

Diphenhydramine HCl, 25 mg
Antihistamine

RELIEVES
• Sneezing
• Runny Nose
• Itchy Throat         
• Itchy, Watery Eyes

48 TABLETS

ACTUAL SIZE

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

DISTRIBUTED BY:
MIDWOOD BRANDS, LLC,
500 VOLVO PKWY
CHESAPEAKE, VA 23320 USA

NOT 100% SATISFIED?
Return within 30 days to the
store of purchase for a refund
(with receipt) or exchange.

*This product is not manufactured or distributed by Kenvue Inc.,
owner of the registered trademark Benadryl® Allergy ULTRATAB®
Tablets. 50844 ORG072132908

Family Wellness 44-329

Family Wellness 44-329

ALLERGY RELIEF 
diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55319-329
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
STARCH, CORN (UNII: O8232NY3SJ)  
D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorpinkScoreno score
ShapeOVALSize11mm
FlavorImprint Code 44;329
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55319-329-224 in 1 CARTON03/02/1990
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:55319-329-082 in 1 CARTON03/02/1990
212 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:55319-329-121 in 1 CARTON03/02/1990
3100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/02/1990
Labeler - Family Dollar Services Inc (024472631)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(55319-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(55319-329) , pack(55319-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(55319-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(55319-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(55319-329)

Revised: 1/2024
Document Id: 89b57910-3363-4560-a3db-6ae94fa0f869
Set id: 358ba91d-06a4-49c9-994d-4e4bf9499dcd
Version: 19
Effective Time: 20240110
 
Family Dollar Services Inc