ALLERGY RELIEF- diphenhydramine hcl tablet, film coated 
United Natural Foods, Inc. dba UNFI

----------

Equaline 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
  • difficulty in urination due to enlargement of the prostate gland
  • glaucoma

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?

1-855-423-2630

Principal Display Panel

EQUALINE®  

NDC 41163-329-22

compare to
Benadryl®
Allergy ULTRATAB®

active ingredient*

allergy relief
diphenhydramine HCl 25 mg
(antihistamine)

relieves:
• sneezing
• itchy, watery eyes
• runny nose
• itchy throat

48 minitabs

actual size

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

*This product is not manufactured or distributed
by Johnson & Johnson Corporation, owner of the
registered trademark Benadryl® Allergy
ULTRATAB®.
50844        REV0721K32922

100% Quality
GUARANTEED

DISTRIBUTED BY UNFI
PROVIDENCE, RI 02908 USA

855-423-2630

Equaline 44-329

Equaline 44-329



ALLERGY RELIEF 
diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-329
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:41163-329-082 in 1 CARTON03/02/1990
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:41163-329-224 in 1 CARTON03/02/1990
212 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:41163-329-121 in 1 CARTON03/02/199001/08/2020
3100 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/02/1990
Labeler - United Natural Foods, Inc. dba UNFI (943556183)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(41163-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(41163-329) , pack(41163-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(41163-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(41163-329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(41163-329)

Revised: 10/2023
Document Id: e2c03f04-f21b-4f70-849c-8b6ae5b6dc1b
Set id: 4517c7ef-156c-42b8-a2da-165e936f0837
Version: 16
Effective Time: 20231021
 
United Natural Foods, Inc. dba UNFI