Loratadine by Chain Drug Consortium, LLC / Aurohealth LLC / Aurobindo Pharma Limited LORATADINE tablet

Loratadine by

Drug Labeling and Warnings

Loratadine by is a Otc medication manufactured, distributed, or labeled by Chain Drug Consortium, LLC, Aurohealth LLC, Aurobindo Pharma Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient (in each tablet)

Loratadine USP 10 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

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 (1-800-222-1222) right away.

Directions

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

Other information

• Tamper-evident: do not use if foil seal under cap, printed with “SEALED for YOUR PROTECTION” is missing, open or broken
• store at 20° to 25°C (68° to 77°F)
• protect from excessive moisture

Inactive ingredients

lactose monohydrate, magnesium stearate, pregelatinized starch (maize), sodium starch glycolate.

Questions or comments?

call 1-855-274-4122

#This product is not manufactured or distributed by Bayer Healthcare LLC distributor of Claritin®.

Distributed By:
Pharmacy Value Alliance LLC
407 East Lancaster Avenue,
Wayne, PA 19087

Made in India
Code: TS/DRUGS/22/2009

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (60 Tablets Bottle)

#COMPARE TO THE ACTIVE
INGREDIENT IN CLARITIN®
Non-Drowsy*
Premier
Value®
Loratadine Tablets USP 10 mg
Allergy Relief
Antihistamine

Indoor & Outdoor
Allergies

24 Hour Relief of:

Sneezing
Runny Nose
Itchy, Watery Eyes
Itchy Throat or Nose 

60 Tablets
*When taken as directed See Drug Facts Panel.

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg Container Carton (60 Tablets)

#COMPARE TO THE ACTIVE
INGREDIENT IN CLARITIN®
Non-Drowsy*

Premier
Value®
Loratadine Tablets USP 10 mg
Allergy
Relief
Antihistamine
Indoor & Outdoor Allergies

24 Hours Relief of:

Sneezing
Runny Nose
Itchy, Watery Eyes
Itchy Throat or Nose

60 Tablets
*When taken as directed
See Drug Facts Panel.
 

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg Blister Carton (30 Tablets)

#COMPARE TO THE ACTIVE
INGREDIENT IN CLARITIN®
Non-Drowsy*

Premier
Value®
Loratadine Tablets USP 10 mg
Allergy Relief
Antihistamine
Indoor & Outdoor
Allergies

24 Hours Relief of:

Sneezing
Runny Nose
Itchy, Watery Eyes
Itchy Throat or Nose

10 Tablets
*When taken as directed See Drug Facts Panel.
 

INGREDIENTS AND APPEARANCE

LORATADINE 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68016-094
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
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, CORN (UNII: O8232NY3SJ)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)

Product Characteristics
Color	WHITE (White to Off-white)	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	39;L
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68016-094-60	1 in 1 CARTON	04/16/2018
1		60 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 68016-094-90	1 in 1 CARTON	04/16/2018
2		90 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 68016-094-10	1 in 1 CARTON	04/16/2018
3		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
4	NDC: 68016-094-30	3 in 1 CARTON	04/16/2018
4		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	ANDA208314	04/16/2018

Labeler - Chain Drug Consortium, LLC (101668460)

Registrant - Aurohealth LLC (078728447)

Establishment
Name	Address	ID/FEI	Business Operations
Aurobindo Pharma Limited		650381903	ANALYSIS(68016-094) , MANUFACTURE(68016-094)