Active Ingredients (In Each Tablet)
Loratadine, USP 10 mg
Pseudoephedrine sulfate, USP 240 mg
The following Structured Product Label (SPL) was submitted to the FDA by Rebel Distributors Corp for the product Loratadine And Pseudoephedrine (NDC 21695-729). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients (in each tablet), purpose, uses, do not use, ask a doctor before use if you have, when using this product do not take more than directed., stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Loratadine, USP 10 mg
Pseudoephedrine sulfate, USP 240 mg
Antihistamine
Nasal decongestant
Taking more than directed may cause drowsiness.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
calcium carbonate, colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, iron oxide black, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, shellac glaze, sodium alginate, sodium citrate, talc and titanium dioxide
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