ALLERGY RELIEF- loratadine capsule, liquid filled

Allergy Relief by

Drug Labeling and Warnings

Allergy Relief by is a Otc medication manufactured, distributed, or labeled by CHAIN DRUG CONSORTIUM. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient (in each capsule)

Loratadine  10mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies

runny nose

sneezing

itchy, water eyes

itching of the nose or throat

Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away

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 (1-800-222-1222).

Directions

• adults and children 6 years and over: 1 capsule daily; not more than 1 capsule in 24 hours
• children under 6 years of age: ask a doctor
• consumers with liver or kidney disease: ask a doctor

Other information

Store between 20-25˚C (68-77˚F)

protect from freezing

retain carton for complete information and warnings

Inactive ingredients

FD&C Blue no. 1, gelatine, mono anddiglyceride of caprilic/capric acid, pharmaceutical ink, polysorbate 80,povidone, purified water, sorbitol, sorbitan solution.

Questions or comments?

1-844-705-4384

PRINCIPAL DISPLAY PANEL

Premier Value®

COMPARE TO THE ACTIVE INGREDIENT IN CLARITIN® LIQUI-GELS®†

*When taken as directed. 

See Drug Facts Panel.

NON-DROWSY*

Allergy Relief

LORATADINE 10 MG 24 HOUR RELIEF

ANTIHISTAMINE

Relieves:

Sneezing

Runny Nose

Itchy, Watery Eyes

Itchy Throar or Nose

Indoor  Outdoor Allergies

10 SOFTGELS**

(**LIQUID-FILLED CAPSULES)

INGREDIENTS AND APPEARANCE

ALLERGY RELIEF 
loratadine capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68016-055
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)	LORATADINE	10 mg

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GELATIN (UNII: 2G86QN327L)
CAPRIC ACID (UNII: 4G9EDB6V73)
POVIDONE K30 (UNII: U725QWY32X)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SORBITAN (UNII: 6O92ICV9RU)

Product Characteristics
Color	blue (Light Blue)	Score	no score
Shape	OVAL (oval shaped)	Size	3mm
Flavor		Imprint Code	21
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68016-055-10	1 in 1 CARTON	12/01/2018	07/31/2025
1		10 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
ANDA	ANDA206214	12/01/2018	07/31/2025

Labeler - CHAIN DRUG CONSORTIUM (101668460)