TRIPROLIDINE HCL DROPS- triprolidine hydrochloride liquid

Triprolidine HCl Drops by

Drug Labeling and Warnings

Triprolidine HCl Drops by is a Otc medication manufactured, distributed, or labeled by Brandywine Pharmaceuticals, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Triprolidine HCl Drops

NDC: 71321-701-50

Active ingredients (in each 2 mL)

Triprolidine HCI 1.25 mg

Purpose

Antihistamine

Uses

■ 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.

Ask a doctor before use if the child has

■ a breathing problem such as emphysema or chronic bronchitis

■ glaucoma

■ trouble urinating due to an enlarged prostate

Ask a doctor before use if the child is

taking sedatives or tranquilizers

When using this product

■ excitability may occur, especially in children

■ marked drowsiness may occur

■ sedatives and tranquilizers may increase the drowsiness effect

Stop use and ask a doctor if

■ new symptoms occur

Keep out of reach of children.

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

Directions

■ use only with enclosed dropper   ■ mL= milliliter

■ do not use dropper for any other drug product

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.

Other information

■ read all product information before using

■ this packaging is child-resistant.

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

Inactive ingredients

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

Questions or comments?

Call 610-314-7943 9 a.m. - 5 p.m. EST.

PRINCIPAL DISPLAY PANEL

NDC: 71321-701-50



Triprolidine HCl Drops



1.69 fl oz (50 mL)

INGREDIENTS AND APPEARANCE

TRIPROLIDINE HCL DROPS 
triprolidine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71321-701
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890) (TRIPROLIDINE - UNII:2L8T9S52QM)	TRIPROLIDINE HYDROCHLORIDE	1.25 mg  in 2 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL (UNII: 506T60A25R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71321-701-50	50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	03/08/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	03/08/2023

Labeler - Brandywine Pharmaceuticals, LLC (080581956)