FLONASE  NIGHTTIME ALLERGY RELIEF- triprolidine hcl tablet 
Haleon US Holdings LLC

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Drug Facts

Active ingredient (in each tablet)

Triprolidine HCl 2.5 mg

Purpose

Uses

  1. runny nose
  2. sneezing
  3. itching of the nose or throat
  4. itchy, watery eyes

Warnings

Ask a doctor before use if you have

Ask a doctor before use if you are taking sedatives or tranquilizers.

When using this product

  • do not exceed recommended dosage
  • excitability may occur, especially in children
  • drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • avoid alcoholic beverages while taking this product
  • be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if new symptoms occur.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Other information

Inactive ingredients

hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinized starch, titanium dioxide

Questions or comments?

1-844-356-6273

Additional Information

KEEP CARTON FOR COMPLETE INFORMATION

Do not use if blister is broken or damaged.

*Dosage is 1 tablet every 4 to 6 hours

Distributed by:

GSK Consumer Healthcare

Warren, NJ 07059

Trademarks are owned by or licensed to the GSK group of companies.

©2022 GSK group of companies or its licensor.

Principal Display Panel

FLONASE

NIGHTTIME ALLERGY RELIEF

NEW INGREDIENT

Triprolidine HCl 2.5 mg - Antihistamine

UP TO
6 HOURS* RELIEF FROM

36TABLETS

080320 – Front Carton

080320 Flonase Nighttime Allergy Relief 36 Tablets
FLONASE   NIGHTTIME ALLERGY RELIEF
triprolidine hcl tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-1329
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890) (TRIPROLIDINE - UNII:2L8T9S52QM) TRIPROLIDINE HYDROCHLORIDE2.5 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
STARCH, CORN (UNII: O8232NY3SJ)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize7mm
FlavorImprint Code FN
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-1329-011 in 1 CARTON12/15/2022
136 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01212/15/2022
Labeler - Haleon US Holdings LLC (079944263)

Revised: 3/2024
Document Id: 14445c6c-88fc-0ac7-e063-6294a90ad9e1
Set id: 070fb5a4-1848-41e8-90bf-57e682de1762
Version: 3
Effective Time: 20240322
 
Haleon US Holdings LLC