ALLERGY RELIEF- diphenhydramine hcl tablet, film coated 
DOLGENCORP, LLC

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Allergy Relief

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
  • 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 years1 tablet
children under 6 yearsdo 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

Principal Display Panel

Since 1903
Rexall®

Allergy Relief
Diphenhydramine HCl, 25 mg
Antihistamine

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

Actual
Size

365
Tablets

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSING

50844 REV0721D32951
Visit us at: Rexall.com or call 1-866-4-REXALL
MANUFACTURED FOR OLD EAST MAIN CO.
100 MISSION RIDGE, GOODLETTSVILLE, TN 37072 USA

Rexall 44-329

Rexall 44-329

ALLERGY RELIEF 
diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-329
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:55910-329-121 in 1 CARTON06/27/2023
1100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:55910-329-51365 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/02/1990
3NDC:55910-329-081 in 1 CARTON03/02/199002/15/2021
324 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/02/1990
Labeler - DOLGENCORP, LLC (068331990)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(55910-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(55910-329) , pack(55910-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(55910-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(55910-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(55910-329)

Revised: 6/2023
Document Id: 35d03036-3185-4af2-ba80-51550eb2e5fa
Set id: 69af44c2-390c-4223-889a-d5555aef5778
Version: 13
Effective Time: 20230627
 
DOLGENCORP, LLC