CHILDRENS PEDIACLEAR PD- triprolidine hydrochloride liquid 
GM Pharmaceuticals, INC

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Children's PediaClear PD

NDC 58809-651-50

Drug Facts

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

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

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

PRINCIPAL DISPLAY PANEL

NDC 58809-651-50
Children’s PediaClear PD Drops

1.69 fl oz (50 mL)

Children’s PediaClear PD Drops Label

Pediaclear PD PDP

Children’s PediaClear PD Drops Drug Facts

Pediaclear PD Drug Facts

Children’s PediaClear PD Drops Carton

Pediaclear PD Drug Facts

CHILDRENS PEDIACLEAR PD 
triprolidine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58809-651
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:58809-651-5050 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product07/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01207/01/2019
Labeler - GM Pharmaceuticals, INC (793000860)

Revised: 3/2024
Document Id: 13918530-d5d1-feba-e063-6294a90a943b
Set id: f3ede5b7-1b0f-493a-b647-4459affc7e54
Version: 8
Effective Time: 20240313
 
GM Pharmaceuticals, INC