ALLERGY RELIEF ANTIHISTAMINE- diphenhydramine hydrochloride capsule, liquid filled

Allergy Relief Antihistamine by

Drug Labeling and Warnings

Allergy Relief Antihistamine by is a Otc medication manufactured, distributed, or labeled by CDMA Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each softgel)

Diphenhydramine HCl 25mg

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     trouble urinating due to an enlarged prostate gland     a breathing problem such as emphysema or chronic bronchitis

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

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

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 softgel
• children 6 to under 12 years: 1 softgel
• children under 6 years of age: do not use this product

Other information

store at room temperature between 20-25°C (68-77°F)    avoid excessive heat, humidity and light

Inactive ingredients

edible white ink, gelatin, glycerin, polyethylene glycol, povidone, purified water, sorbitol sorbitan solution

Questions or Comments?

Call: 1-888-577-8033 Monday - Friday 9am-4:30pm EST

SPL UNCLASSIFIED SECTION

QC®
QUALITY CHOICE

*Compare to the active Ingredient in BENADRYL® Allergy LIQUI-GELS®

Dye-Free

Relieves sneezing
Itchy, watery eyes
Runny nose
Itchy throat

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 McNeil Consumer Healthcare, distributor of Benadryl®,or Catalent Pharma Solutions, Inc., owner of the registered trademark LIQUI-GELS®.

QC 100% SATISFACTION GUARANTEED

Distributed by C.D.M.A., Inc.©
43157 W 9 Mile Rd
Novi, MI 48375
www.qualitychoice.com
Questions: 800-935-2362

Product of UAE

Packaged and Quality assured in USA

READ AND KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

REV.01-092022

Packaging

INGREDIENTS AND APPEARANCE

ALLERGY RELIEF ANTIHISTAMINE 
diphenhydramine hydrochloride capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-474
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, UNSPECIFIED (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SORBITAN (UNII: 6O92ICV9RU)

Product Characteristics
Color	WHITE (clear)	Score	no score
Shape	CAPSULE	Size	15mm
Flavor		Imprint Code	783
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-474-24	2 in 1 CARTON	05/01/2021
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	05/01/2021

Labeler - CDMA Inc (011920774)