Loratadine Allergy Relief description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Loratadine Allergy Relief

Clinical Solutions Wholesale
Clinical Solutions Wholesale


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT(S)

Loratadine USP, 10 mg

PURPOSE

Antihistamine

USE(S)

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

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 and kidney disease

ask a doctor

OTHER INFORMATION

  • •store between 20 and 25° C (68 and 77° F)
  • •protect from excessive moisture
  • TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.

INACTIVE INGREDIENTS

Corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

QUESTIONS?

Call 1-800-406-7984

PRINCIPAL DISPLAY PANEL

Package/Label Display Panel

Package/Label Display Panel

Package/Label Display Panel

Loratadine Allergy Relief

Loratadine TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:58118-0526(NDC:51660-526)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LORATADINE loratadine 10 mg

Inactive Ingredients

Ingredient Name Strength
STARCH, CORN
lactose monohydrate
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
white (White to Off White) 6 mm RX526 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58118-0526-9 90 in 1 BOTTLE, PLASTIC
2 NDC:58118-0526-8 30 in 1 BLISTER PACK
3 NDC:58118-0526-0 1 in 1 PACKET
4 NDC:58118-0526-3 30 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076134 2003-08-28


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.