LORATADINE ODT- loratadine tablet, orally disintegrating

Država: Združene države Amerike

Jezik: angleščina

Source: NLM (National Library of Medicine)

Aktivna sestavina:

LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)

Dostopno od:

Chain Drug Consortium, LLC

Pot uporabe:

ORAL

Tip zastaranja:

OTC DRUG

Terapevtske indikacije:

Antihistamine temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: - runny nose - sneezing - itchy, watery eyes - itching of the nose or throat if you have ever had an allergic reaction to this product or any of its ingredients. liver or kidney disease. Your doctor should determine if you need a different dose. an allergic reaction to this product occurs. Seek medical help right away.

Status dovoljenje:

Abbreviated New Drug Application

Lastnosti izdelka

LORATADINE ODT - LORATADINE TABLET, ORALLY DISINTEGRATING
CHAIN DRUG CONSORTIUM, LLC
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LORATADINE ORALLY DISINTEGRATING TABLETS USP 10 MG
_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
sneezing
itchy, watery 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 (1-800-222-
1222) right away.
DIRECTIONS
place 1 tablet on tongue; tablet disintegrates, with or without water
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_
Phenylketonurics: Contains phenylalanine 2.25 mg per tablet
do not use if the individual blister unit is open or torn
store at 20° to 25°C (68° to 77°F)
use tablet immediately after opening individual blister
Complies with USP test 2 for Disintegration
_INACTIVE INGREDIENTS_
aspartame, crospovidone, mannitol, microcrystalline cellulose,
peppermint,
pregelatinized starch (maize), sodium stearyl fumarate
_QUESTIONS OR COMMENTS?_
call 1-855-274-4122
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 MG, BLISTER CARTON 10
ORALLY
DISINTEGRATING TABLETS
NDC 68016-088-10
**COMPARE TO THE ACTIVE INGREDIENT
IN CLARITIN REDITABS
Original Prescription Strength
Non-Drowsy*
PREMIER VALUE
LORATADINE ORALLY DISINTEGRATING TABL