ALLERGY- diphenhydramine hcl tablet, film coated 
Kroger Company

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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Kroger 44-329 Delisted

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:
    • sneezing
    • itchy, watery eyes
    • runny nose
    • itching of the nose or throat
  • temporarily relieves these symptoms due to the common cold:
    • sneezing
    • runny nose

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

  • 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 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 25°C (77°F); 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?

1-800-632-6900

Principal display panel

COMPARE TO the active ingredient of
BENADRYL® ALLERGY ULTRATAB® TABLETS
*See bottom panel

NDC 30142-329-90

Kroger®

Allergy
Tablets

Diphenhydramine HCl,
25 mg
Antihistamine

OUR PHARMACIST RECOMMENDED

actual
size

RELIEVES:
Sneezing
Runny Nose
Itchy, Watery Eyes
Itchy Throat

48 TABLETS

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

*Benadryl® is a registered trademark of Johnson & Johnson
Corporation, New Brunswick, NJ 08933. Johnson & Johnson
Corporation is not affiliated with The Kroger Co. or this product.
50844 REV1016A32922

DISTRIBUTED BY
THE KROGER CO.
CINCINNATI, OHIO 45202
QUALITY GUARANTEE
800-632-6900
www.kroger.com

Kroger 44-329

Kroger 44-329

ALLERGY 
diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-329
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)  
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)  
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:30142-329-082 in 1 CARTON06/01/201906/11/2023
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:30142-329-121 in 1 CARTON06/01/201906/11/2023
2100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:30142-329-904 in 1 CARTON06/01/201906/11/2023
312 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:30142-329-051 in 1 CARTON06/01/201905/19/2023
4400 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34106/01/201906/11/2023
Labeler - Kroger Company (006999528)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(30142-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(30142-329) , pack(30142-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(30142-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(30142-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(30142-329)

Revised: 7/2023
 
Kroger Company