ALLERGY RELIEF- diphenhydramine hcl capsule, liquid filled 
Topco Associates, LLC

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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TopCare 44-658-Delisted

Active ingredient (in each liquid-filled capsule)

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
    • runny nose
    • itchy, watery eyes
    • sneezing
    • itching of the nose or throat
  • temporarily relieves these symptoms due to the common cold:
    • runny nose
    • sneezing

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 (1-800-222-1222) right away.

Directions

  • take every 4 to 6 hours
  • do not take more than 6 doses in 24 hours
adults and children 12
years of age and over		1 to 2 capsules
children 6 to under 12
years of age		1 capsule
children under 6 years
of age		do not use this
product in children
under 6 years of age

Other information

  • 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 heat, humidity and light
  • see end flap for expiration date and lot number

Inactive ingredients

edible white ink, gelatin, glycerin, lecithin, mineral oil, polyethylene glycol, purified water, sorbitol

Questions or comments?

1-888-423-0139

Principal display panel

TopCare
      Health™

NDC 36800-658-08

COMPARE TO BENADRYL®
DYE-FREE ALLERGY LIQUI-GELS®
ACTIVE INGREDIENT*

DYE-FREE

Allergy Relief
DIPHENHYDRAMINE HCl 25 mg - Antihistamine

RELIEF OF:

• Sneezing

• Runny nose

• Itchy, Watery Eyes

• Itchy, Nose or Throat

Our Pharmacists Recommend

24 SOFTGELS**
** Liquid Filled Capsules

actual size

DISTRIBUTED BY TOPCO ASSOCIATES LLC
ELK GROVE VILLAGE, IL 60007
©TOPCO LNKA0219 QUESTIONS? 1-888-423-0139
topcare@topco.com www.topcarebrand.com

PRODUCT OF CHINA 
PACKAGED AND QUALITY ASSURED IN THE USA

*This product is not manufactured or distributed by
McNeil Consumer Healthcare, owner of the registered
trademark Benadryl® Dye-Free Allergy LIQUI-GELS®.

50844 ORG061465808

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

Topcare 44-658

Topcare 44-658

ALLERGY RELIEF 
diphenhydramine hcl capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-658
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
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
ColorYELLOW (clear) Scoreno score
ShapeOVALSize15mm
FlavorImprint Code 658
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36800-658-082 in 1 CARTON06/15/201911/06/2022
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34106/15/201911/06/2022
Labeler - Topco Associates, LLC (006935977)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837PACK(36800-658)

Revised: 3/2021
Document Id: bb505740-a4c6-449b-91a5-cfd019612439
Set id: 283c00bc-5b10-47c0-a51d-0f3dd59b41d5
Version: 3
Effective Time: 20210315
 
Topco Associates, LLC