ALLERGY RELIEF- diphenhydramine hcl capsule, liquid filled

Allergy Relief by

Drug Labeling and Warnings

Allergy Relief by is a Otc medication manufactured, distributed, or labeled by Topco Associates, LLC, LNK International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 12years of age and over: 1 to 2 capsules
• children 6 to under 12years of age: 1 capsule
• children under 6 yearsof 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

INGREDIENTS AND APPEARANCE

ALLERGY RELIEF 
diphenhydramine hcl capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 36800-658
Route of Administration	ORAL

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
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
Color	YELLOW (clear)	Score	no score
Shape	OVAL	Size	15mm
Flavor		Imprint Code	658
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 36800-658-08	2 in 1 CARTON	06/15/2019
1		12 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part341	06/15/2019

Labeler - Topco Associates, LLC (006935977)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		832867837	PACK(36800-658)