ALLERGY RELIEF- loratadine capsule, liquid filled 
CHAIN DRUG MARKETING ASSOCIATION INC.

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1195A - QCH - 2018-0103

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 children6 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 product information

Inactive ingredients

FD&C blue #1, gelatin, mono and diglyceride of caprilic/capric acid, pharmaceutical ink, polysorbate 80, povidone, purified water, sorbitol, sorbitan solution.

Questions or Comments?

1-844-705-4384

PRINCIPAL DISPLAY PANEL

Quality Choice®

NDC 63868-669-10

*Compare to the Active Ingredient in CLARITIN® Liqui-Gels®

Non-Drowsy†

Allergy Relief

Loratadine 10 mg | Antihistamine

Indoor & Outdoor Allergies

Relief of:

Sneezing | Runny Nose

Itchy, Watery Eyes

Itchy Throat or Nose

24 Hour

†When taken as directed. See Drug Facts Panel.

10 Softgels**

**Liquid-Filled Capsules

image description

ALLERGY RELIEF 
loratadine capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-669
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
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
Colorblue (Light Blue) Scoreno score
ShapeOVAL (oval shaped) Size3mm
FlavorImprint Code 21
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-669-101 in 1 CARTON09/01/2018
110 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20621409/01/2018
Labeler - CHAIN DRUG MARKETING ASSOCIATION INC. (011920774)

Revised: 1/2019
Document Id: 7e9542d0-f6b9-7156-e053-2a91aa0a9a16
Set id: 18eaaeb7-1408-4621-bf88-1dc5cb06a9b3
Version: 1
Effective Time: 20190103
 
CHAIN DRUG MARKETING ASSOCIATION INC.