CLEMASTINE FUMARATE CLEMASTINE FUMARATE CHARTWELL RX, LLC FDA Approved Each teaspoonful (5 mL) of Clemastine Fumarate Syrup for oral administration contains clemastine 0.5 mg (present as clemastine fumarate, USP 0.67 mg). Other ingredients: alcohol 5.5% v/v, wild cherry flavor, fumaric acid, methylparaben, propylene glycol, propylparaben, purified water, saccharin sodium, sodium hydroxide, and sorbitol solution. Clemastine fumarate belongs to the benzhydryl ether group of antihistaminic compounds. The chemical name is (+)-(2R)-2-[2-[[(R)-p-Chloro-α-methyl-α-phenylbenzyl]- oxy]ethyl]-1-methylpyrrolidine fumarate and has the following structural formula: C 21 H 26 CINO.C 4 H 4 O 4 M.W. 459.97 CAS Registration Number 145976-57-9 Clemastine fumarate occurs as a colorless to faintly yellow, practically odorless, crystalline powder. Clemastine Fumarate Syrup is a clear, colorless liquid with wild cherry flavor and has an approximate pH of 6.2. "Image Description"
FunFoxMeds bottle
Route
ORAL
Applications
ANDA074884
Package NDC

Drug Facts

Composition & Profile

Strengths
0.5 mg/5 ml 0.67 mg/5 ml 120 ml
Quantities
5 ml 120 ml
Treats Conditions
Indications And Usage Clemastine Fumarate Syrup Is Indicated For The Relief Of Symptoms Associated With Allergic Rhinitis Such As Sneezing Rhinorrhea Pruritus And Lacrimation Clemastine Fumarate Syrup Is Indicated For Use In Pediatric Populations Age 6 Years Through 12 And Adults See Dosage And Administration It Should Be Noted That Clemastine Fumarate Is Indicated For The Relief Of Mild Uncomplicated Allergic Skin Manifestations Of Urticaria And Angioedema At The 2 Mg Dosage Level Only

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UPC
0362135713416
UNII
19259EGQ3D
Packaging

HOW SUPPLIED Clemastine Fumarate Syrup: clemastine 0.5 mg/5 mL (present as clemastine fumarate, USP 0.67 mg/5 mL). A clear, colorless liquid with wild cherry flavor, in 120 mL bottle. 120 mL bottle (NDC 62135-713-41) Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Manufactured for: Chartwell RX, LLC. Congers, NY 10920 L71572 Rev. 07/2023; PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Clemastine Fumarate Syrup, 0.5mg/5ml - NDC-62135-713-41 - 120 ml Bottle label. "Image Description"

Package Descriptions
  • HOW SUPPLIED Clemastine Fumarate Syrup: clemastine 0.5 mg/5 mL (present as clemastine fumarate, USP 0.67 mg/5 mL). A clear, colorless liquid with wild cherry flavor, in 120 mL bottle. 120 mL bottle (NDC 62135-713-41) Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Manufactured for: Chartwell RX, LLC. Congers, NY 10920 L71572 Rev. 07/2023
  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Clemastine Fumarate Syrup, 0.5mg/5ml - NDC-62135-713-41 - 120 ml Bottle label. "Image Description"

Overview

Each teaspoonful (5 mL) of Clemastine Fumarate Syrup for oral administration contains clemastine 0.5 mg (present as clemastine fumarate, USP 0.67 mg). Other ingredients: alcohol 5.5% v/v, wild cherry flavor, fumaric acid, methylparaben, propylene glycol, propylparaben, purified water, saccharin sodium, sodium hydroxide, and sorbitol solution. Clemastine fumarate belongs to the benzhydryl ether group of antihistaminic compounds. The chemical name is (+)-(2R)-2-[2-[[(R)-p-Chloro-α-methyl-α-phenylbenzyl]- oxy]ethyl]-1-methylpyrrolidine fumarate and has the following structural formula: C 21 H 26 CINO.C 4 H 4 O 4 M.W. 459.97 CAS Registration Number 145976-57-9 Clemastine fumarate occurs as a colorless to faintly yellow, practically odorless, crystalline powder. Clemastine Fumarate Syrup is a clear, colorless liquid with wild cherry flavor and has an approximate pH of 6.2. "Image Description"

Indications & Usage

Clemastine Fumarate Syrup is indicated for the relief of symptoms associated with allergic rhinitis such as sneezing, rhinorrhea, pruritus and lacrimation. Clemastine Fumarate Syrup is indicated for use in pediatric populations (age 6 years through 12) and adults (see DOSAGE AND ADMINISTRATION ). It should be noted that clemastine fumarate is indicated for the relief of mild uncomplicated allergic skin manifestations of urticaria and angioedema at the 2 mg dosage level only.

Dosage & Administration

DOSAGE SHOULD BE INDIVIDUALIZED ACCORDING TO THE NEEDS AND RESPONSE OF THE PATIENT. Pediatric: Children aged 6 to 12 years: For Symptoms Of Allergic Rhinitis -The starting dose is 1 teaspoonful (0.5 mg clemastine) twice daily. Since single doses of up to 2.25 mg clemastine were well tolerated by this age group, dosage may be increased as required, but not to exceed 6 teaspoonfuls daily (3 mg clemastine). For Urticaria and Angioedema -The starting dose is 2 teaspoonfuls (1 mg clemastine) twice daily, not to exceed 6 teaspoonfuls daily (3 mg clemastine). Adults and Children 12 years and Over: For Symptoms Of Allergic Rhinitis -The starting dose is 2 teaspoonfuls (1.0 mg clemastine) twice daily. Dosage may be increased as required, but not to exceed 12 teaspoonfuls daily (6 mg clemastine). For Urticaria and Angioedema -The starting dose is 4 teaspoonfuls (2 mg clemastine) twice daily, not to exceed 12 teaspoonfuls daily (6 mg clemastine).

Warnings & Precautions
WARNINGS Antihistamines should be used with considerable caution in patients with: narrow angle glaucoma, stenosing peptic ulcer, pyloroduodenal obstruction, symptomatic prostatic hypertrophy, and bladder neck obstruction. Use with CNS Depressants: Clemastine fumarate has additive effects with alcohol and other CNS depressants (hypnotics, sedatives, tranquilizers, etc.) Use in Activities Requiring Mental Alertness: Patients should be warned about engaging in activities requiring mental alertness such as driving a car or operating appliances, machinery, etc. Use in the Elderly (approximately 60 years or older): Antihistamines are more likely to cause dizziness, sedation, and hypotension in elderly patients.
Contraindications

Antihistamines are contraindicated in patients hypersensitive to the drug or to other antihistamines of similar chemical structure (see PRECAUTIONS - Drug Interactions ). Antihistamines should not be used in newborn or premature Infants. Because of the higher risk of antihistamines for infants generally and for newborns and prematures in particular, antihistamine therapy is contraindicated in nursing mothers (See PRECAUTIONS - Nursing Mothers ).

Adverse Reactions

The most frequent adverse reactions are underlined: Nervous System: Sedation, sleepiness, dizziness, disturbed coordination , fatigue, confusion, restlessness, excitation, nervousness, tremor, irritability, insomnia, euphoria, paresthesia, blurred vision, diplopia, vertigo, tinnitus, acute labyrinthitis, hysteria, neuritis, convulsions. Gastrointestinal System: Epigastric distress , anorexia, nausea, vomiting, diarrhea, constipation. Respiratory System: Thickening of bronchial secretions , tightness of chest and wheezing, nasal stuffiness. Cardiovascular System: Hypotension, headache, palpitations, tachycardia, extrasystoles. Hematologic System: Hemolytic anemia, thrombocytopenia, agranulocytosis. Genitourinary System: Urinary frequency, difficult urination, urinary retention, early menses. General : Urticaria, drug rash, anaphylactic shock, photosensitivity, excessive perspiration, chills, dryness of mouth, nose and throat.


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