ALLERGY RELIEF- loratadine capsule, liquid filled 
CHAIN DRUG CONSORTIUM

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1195A-PRV-2020-0903

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 over1 capsule daily; not more than 1 capsule in 24 hours
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask 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)

image description

ALLERGY RELIEF 
loratadine capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-055
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:68016-055-101 in 1 CARTON12/01/2018
110 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20621412/01/2018
Labeler - CHAIN DRUG CONSORTIUM (101668460)

Revised: 9/2020
Document Id: af0f9bd2-3b77-967a-e053-2995a90a9f6a
Set id: c63bbb89-9125-42da-b652-36c32b839df3
Version: 2
Effective Time: 20200911
 
CHAIN DRUG CONSORTIUM