TRIPROLIDINE HCL DROPS- triprolidine hydrochloride liquid 
Brandywine Pharmaceuticals, LLC

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Triprolidine HCl Drops

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)

LabelCartonPeel_Back

TRIPROLIDINE HCL DROPS 
triprolidine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71321-701
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890) (TRIPROLIDINE - UNII:2L8T9S52QM) TRIPROLIDINE HYDROCHLORIDE1.25 mg  in 2 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71321-701-5050 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product03/08/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/08/2023
Labeler - Brandywine Pharmaceuticals, LLC (080581956)

Revised: 1/2024
Document Id: 0e775b4a-84df-ff58-e063-6394a90a64f7
Set id: f66a4235-d1a5-d2fa-e053-2a95a90a67f9
Version: 3
Effective Time: 20240108
 
Brandywine Pharmaceuticals, LLC