Loratadine by Sunmark LORATADINE tablet

Loratadine by

Drug Labeling and Warnings

Loratadine by is a Otc medication manufactured, distributed, or labeled by Sunmark. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

• Safety sealed: do not use if printed foil under cap is broken or missing. (for bottle only)
• Safety sealed: do not use if the imprinted blister unit is open or torn. (for blister package only)

• Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
• Protect from excessive moisture. (for blister package only)

Inactive Ingredients

Lactose monohydrate, magnesium stearate, microcrystalline cellulose and sodium starch glycolate.

Questions or comments?

1-800- 206-7821

01-2016M

Distributed by McKesson

One Post Street, San Francisco, CA 94104

10 mg Label

sunmark®

COMPARE TO CLARITIN® TABLETS

ACTIVE INGREDIENT**

NDC: 49348-112-44

24 Hour

loratadine

tablets, USP 10 mg

Antihistamine

*When taken

as directed.

See drug

facts panel.

GLUTEN FREE

24 hour relief of sneezing, runny nose,

itchy, watery eyes, itchy throat or nose

Indoor and Outdoor Allergies

NON-DROWSY*

SAFETY SEALED: DO NOT USE IF PRINTED

FOIL UNDER CAP IS BROKEN OR MISSING.

30 TABLETS

INGREDIENTS AND APPEARANCE

LORATADINE 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49348-112
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)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
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	GG296
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49348-112-44	1 in 1 CARTON	06/01/2016	10/31/2020
1		30 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 49348-112-13	1 in 1 CARTON	06/01/2016	10/31/2020
2		90 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 49348-112-01	1 in 1 CARTON	06/01/2016	05/31/2019
3		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	ANDA075209	06/01/2016	10/31/2020

Labeler - Sunmark (177667227)