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FDA LABEL GENERIC: Triprolidine MFR: GM Pharmaceuticals, INC

Triprolidine Hcl 0.625 Mg In 1 Ml Oral Solution

NDC 58809-651-50

Drug Facts

Triprolidine HCI 1.25 mg

Antihistamine

INDICATIONS AND USAGE

■ temporarily relieves these symptoms due to hay fever

(allergic rhinitis) or other upper respiratory allergies:

■ runny nose ■ itching of the nose or throat

■ sneezing ■ itchy, watery eyes

WARNINGS

Do not exceed recommended dosage.

■ a breathing problem such as emphysema or chronic bronchitis

■ glaucoma

taking sedatives or tranquilizers

■ excitability may occur, especially in children

■ marked drowsiness may occur

■ sedatives and tranquilizers may increase the drowsiness effect

■ new symptoms occur

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE AND ADMINISTRATION

■ use only with enclosed dropper   ■ mL= milliliter

■ do not use dropper for any other drug product

Age Dose
Children 6 to under 12 years: 2 mL every 6 hours, not to exceed 4 doses in 24 hours, or as directed by a doctor.
Children under 6: Ask a doctor.

■ read all product information before using

■ this packaging is child-resistant.

■ store at room temperature 20-30°C (68-86°F)

citric acid anhydrous, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sodium saccharin, sorbitol solution

Call 1-888-535-0305 9 a.m. - 5 p.m. CST.

ASK A DOCTOR

NDC 58809-651-50
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