Loratadine Tablets Usp 10 Mg

Loratadine Tablets Usp 10 Mg
SPL v2
SPL
SPL Set ID 98e41ae1-677a-4583-9a0a-edba29ebbc30
Route
ORAL
Published
Effective Date 2024-06-29
Document Type 34390-5 Human OTC Drug Label

Drug Facts

Composition & Product

Active Ingredients
Loratadine (10 mg)
Inactive Ingredients
Lactose Monohydrate Magnesium Stearate Starch, Corn Sodium Starch Glycolate Type A Potato

Identifiers & Packaging

Pill Appearance
Imprint: 39;L Shape: round Color: white Size: 6 mm Score: 1
Marketing Status
ANDA Active Since 2024-02-23

Description

Loratadine USP 10 mg

Purpose

Antihistamine


Medication Information

Purpose

Antihistamine

Description

Loratadine USP 10 mg

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.

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



Distributed by:

MAJOR®  PHARMACEUTICALS

Indianapolis, IN 46268

(800) 616-2471

www.majorpharmaceuticals.com



Made in India

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.

Active Ingredient (in Each Tablet)

Loratadine USP 10 mg

Ask A Doctor Before Use If You Have

liver or kidney disease. Your doctor should determine if you need a different dose.

Package Label Principal Display Panel 10 Mg (30 Tablets Bottle)

MAJOR®



NDC 0904-7426-46



Non-Drowsy*

Loratadine Tablets USP

10 mg

Antihistamine



24 Hour   |    Indoor & Outdoor Allergies



Relief of:

  • Sneezing
  • Runny Nose
  • Itchy, Watery Eyes
  • Itchy Throat or Nose

30 Tablets



*When taken as directed. See Drug Facts Panel.





Package Label Principal Display Panel 10 Mg Container Carton (30 Tablets)

MAJOR®



NDC 0904-7426-46

Compare to the

active ingredient

in Claritin®†



Non-Drowsy*

Loratadine

Tablets USP

10 mg

Antihistamine



Indoor & Outdoor Allergies

24 Hour



Relief of:

•    Sneezing

•    
Runny Nose

•    Itchy, Watery Eyes

•    Itchy Throat or Nose



30 Tablets

*When taken as directed. See Drug Facts Panel.




Structured Label Content

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
Purpose

Antihistamine

Warnings

Do not use



if you have ever had an allergic reaction to this product or any of its ingredients.

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 (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 (Inactive ingredients)

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

Questions Or Comments? (Questions or comments?)


call 1-855-274-4122



Distributed by:

MAJOR®  PHARMACEUTICALS

Indianapolis, IN 46268

(800) 616-2471

www.majorpharmaceuticals.com



Made in India

When Using This Product (When using this product)

do not take more than directed. Taking more than directed may cause drowsiness.

Stop Use and Ask A Doctor If (Stop use and ask a doctor if)

an allergic reaction to this product occurs. Seek medical help right away.

If Pregnant Or Breast Feeding, (If pregnant or breast-feeding,)

ask a health professional before use.

Keep Out of Reach of Children. (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.

Active Ingredient (in Each Tablet) (Active ingredient (in each tablet))

Loratadine USP 10 mg

Ask A Doctor Before Use If You Have (Ask a doctor before use if you have)

liver or kidney disease. Your doctor should determine if you need a different dose.

Package Label Principal Display Panel 10 Mg (30 Tablets Bottle) (PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30 Tablets Bottle))

MAJOR®



NDC 0904-7426-46



Non-Drowsy*

Loratadine Tablets USP

10 mg

Antihistamine



24 Hour   |    Indoor & Outdoor Allergies



Relief of:

  • Sneezing
  • Runny Nose
  • Itchy, Watery Eyes
  • Itchy Throat or Nose

30 Tablets



*When taken as directed. See Drug Facts Panel.





Package Label Principal Display Panel 10 Mg Container Carton (30 Tablets) (PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg Container Carton (30 Tablets))

MAJOR®



NDC 0904-7426-46

Compare to the

active ingredient

in Claritin®†



Non-Drowsy*

Loratadine

Tablets USP

10 mg

Antihistamine



Indoor & Outdoor Allergies

24 Hour



Relief of:

•    Sneezing

•    
Runny Nose

•    Itchy, Watery Eyes

•    Itchy Throat or Nose



30 Tablets

*When taken as directed. See Drug Facts Panel.




Advanced Ingredient Data


Raw Label Data

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