Claritin-D ® 24 Hour

Claritin-D by

Drug Labeling and Warnings

Claritin-D by is a Otc medication manufactured, distributed, or labeled by REMEDYREPACK INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CLARITIN-D 24 HOUR- loratadine and pseudoephedrine sulfate tablet, extended release 
REMEDYREPACK INC.

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Claritin-D ®



24 Hour

Drug Facts

Active ingredient (in each tablet)	Purpose
Loratadine 10 mg	Antihistamine
Pseudoephedrine sulfate 240 mg	Nasal decongestant

Uses

• temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
• sneezing
• itchy, watery eyes
• runny nose
• itching of the nose or throat
• temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
• reduces swelling of nasal passages
• temporarily relieves sinus congestion and pressure
• temporarily restores freer breathing through the nose

Warnings

Do not use

• if you have ever had an allergic reaction to this product or any of its ingredients
• if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

• heart disease
• thyroid disease
• high blood pressure
• diabetes
• trouble urinating due to an enlarged prostate gland
• 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.
• symptoms do not improve within 7 days or are accompanied by a fever
• nervousness, dizziness or sleeplessness occurs

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.

Directions

• do not divide, crush, chew or dissolve the tablet

• adults and children 12 years and over: 1 tablet daily with a full glass of water; not more than 1 tablet in 24 hours
• children under 12 years of age: ask a doctor
• consumers with liver or kidney disease: ask a doctor

Other information

• each tablet contains: calcium 25 mg
• safety sealed: do not use if the individual blister unit imprinted with Claritin-D ® 24 hour is open or torn
• store between 20° to 25°C (68° to 77°F)
• protect from light and store in a dry place

Inactive ingredients

carnauba wax, dibasic calcium phosphate dihydrate, ethylcellulose, hydroxypropyl cellulose, hypromellose, magnesium stearate, pharmaceutical ink, polyethylene glycol, povidone, silicon dioxide, sucrose, titanium dioxide

Questions or comments?

1-800-CLARITIN (1-800-252-7484) or www.claritin.com

DRUG: Claritin-D24 Hour 24 Hour

GENERIC: Loratadine and pseudoephedrine sulfate

DOSAGE: TABLET, EXTENDED RELEASE

ADMINSTRATION: ORAL

NDC: 70518-2761-0

COLOR: white

SHAPE: ROUND

SCORE: No score

SIZE: 18 mm

IMPRINT: Claritin;D;24

PACKAGING: 5 in 1 BLISTER PACK

OUTER PACKAGING: 3 in 1 CARTON

ACTIVE INGREDIENT(S):

• PSEUDOEPHEDRINE SULFATE 240mg in 1
• LORATADINE 10mg in 1

INACTIVE INGREDIENT(S):

• CARNAUBA WAX
• CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE
• HYPROMELLOSES
• ETHYLCELLULOSES
• HYDROXYPROPYL CELLULOSE (1600000 WAMW)
• MAGNESIUM STEARATE
• POLYETHYLENE GLYCOL, UNSPECIFIED
• POVIDONE
• SILICON DIOXIDE
• SUCROSE
• TITANIUM DIOXIDE

CLARITIN-D  24 HOUR
loratadine and pseudoephedrine sulfate tablet, extended release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70518-2761(NDC: 11523-4332)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)	LORATADINE	10 mg
PSEUDOEPHEDRINE SULFATE (UNII: Y9DL7QPE6B) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F)	PSEUDOEPHEDRINE SULFATE	240 mg

Inactive Ingredients
Ingredient Name	Strength
CARNAUBA WAX (UNII: R12CBM0EIZ)
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)
HYPROMELLOSES (UNII: 3NXW29V3WO)
ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SUCROSE (UNII: C151H8M554)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	white (white to off-white)	Score	no score
Shape	ROUND	Size	18mm
Flavor		Imprint Code	Claritin;D;24
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70518-2761-0	3 in 1 CARTON	05/29/2020	10/16/2023
1		5 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
NDA	NDA020470	05/29/2020	10/16/2023

Labeler - REMEDYREPACK INC. (829572556)

Revised: 10/2023

Document Id: 07d728ef-c115-6460-e063-6294a90a846f

34390-5

Set id: a1d6f8e5-169e-48aa-a264-e0f4845e801d

Version: 5

Effective Time: 20231016