ALLERGY RELIEF- diphenhydramine hcl tablet, film coated 
H E B

----------

HEB 44-329

Active ingredient (in each tablet)

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

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

adults and children 12 years and over1 to 2 tablets
children 6 to under 12 years
1 tablet
children under 6 years
do not use

Other information

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?

1-800-426-9391

Principal display panel

Compare to Benadryl®Allergy ULTRATAB® 
Tablets
active ingredient*

NDC 37808-932-08

H-E-B®

Allergy Relief
Diphenhydramine HCl, 25 mg
Antihistamine

Allergy

Relief of:
• Sneezing
• Runny nose
• Itchy, watery eyes
• Itchy throat

24 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

100%                     If you aren't completely pleased       
GUARANTEE |     
with this product, we'll be happy to
promise               
 replace it or refund your money.
                                    
You have our word on it.

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

50844 REV0721B32908

MADE WITH PRIDE AND CARE FOR H-E-B®, SAN ANTONIO, TX 78204

HEB 44-329

HEB 44-329

ALLERGY RELIEF 
diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-932
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:37808-932-082 in 1 CARTON03/02/1990
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:37808-932-78600 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/02/1990
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/02/1990
Labeler - H E B (007924756)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(37808-932)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(37808-932) , pack(37808-932)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(37808-932)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(37808-932)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(37808-932)

Revised: 1/2024
Document Id: 46a5b70f-04eb-46b9-9305-ae706aba0cb4
Set id: c9e977b6-fba6-49ea-9d80-b43b0842bbe1
Version: 11
Effective Time: 20240126
 
H E B