ANTIHISTAMINE ALLERGY- diphenhydramine hydrochloride capsule, coated 
H E B

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.

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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

  • glaucoma

  • a breathing problem such as emphysema or chronic bronchitis

  • 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 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 of age and over

1 to 2 tablets 
 children 6 to under 12 years of age  1 tablet   
 children under 6 years of age  do not use this product in children under 6 years of age

Other information

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

Principal Display Panel

Compare to Benadryl® Allergy Ultratab® active ingredient*

NDC 37808-329-08

H-E-B®

ANTIHISTAMINE ALLERGY
For Allergy Relief
Diphenhydramine Hydrochloride, 25 mg

• Sneezing            • Itchy, watery eyes
• Runny Nose       • Itchy throat

Does Not Contain Gluten

24 Tablets

*This product is not manfucatured or distributed by McNeil Consumer Healthcare, owner of the registered Benadryl® Allergy Ultratab®.
50844        ORG051232908        1212

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

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

HEB 44-329

HEB 44-329

ANTIHISTAMINE ALLERGY 
diphenhydramine hcl capsule, coated
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-329
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
D&C RED NO. 27 (UNII: 2LRS185U6K)  
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL (UNII: 532B59J990)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Color PINK Score no score
Shape CAPSULE Size 11mm
Flavor Imprint Code 44;329
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37808-329-08 2 in 1 CARTON
1 12 in 1 BLISTER PACK
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part341 03/02/1990
Labeler - H E B (007924756)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 038154464 PACK(37808-329)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 832867894 MANUFACTURE(37808-329)

Revised: 2/2013
Document Id: 469f4511-61e0-4a1a-b450-ae0f3aa1a67d
Set id: be8bdf33-3cc2-43a8-bcd3-8e273b2f8972
Version: 1
Effective Time: 20130225
 
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