FLONASE Nighttime Allergy Relief

Generic: triprolidine hcl

Labeler: Haleon US Holdings LLC
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive

Drug Facts

Product Profile

Brand Name FLONASE Nighttime Allergy Relief
Generic Name triprolidine hcl
Labeler Haleon US Holdings LLC
Dosage Form TABLET
Routes
ORAL
Active Ingredients

TRIPROLIDINE HYDROCHLORIDE 2.5 mg/1

Identifiers & Regulatory

Product NDC 0135-1329
Product ID 0135-1329_669165f1-6d53-4020-8f01-fbd9cb09c99b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2022-12-15
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01351329
Hyphenated Format 0135-1329

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name FLONASE Nighttime Allergy Relief (source: ndc)
Generic Name triprolidine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (0135-1329-01) / 36 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0135-1329-01 1 BLISTER PACK in 1 CARTON (0135-1329-01) / 36 TABLET in 1 BLISTER PACK

Ingredients (1)

TRIPROLIDINE HYDROCHLORIDE (2.5 mg/1)

Linked Drug Pages (1)

FLONASE Nighttime Allergy Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "669165f1-6d53-4020-8f01-fbd9cb09c99b", "openfda": {"unii": ["YAN7R5L890"], "rxcui": ["1099694", "2623978"], "spl_set_id": ["070fb5a4-1848-41e8-90bf-57e682de1762"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0135-1329-01)  / 36 TABLET in 1 BLISTER PACK", "package_ndc": "0135-1329-01", "marketing_end_date": "20260228", "marketing_start_date": "20221215"}], "brand_name": "FLONASE Nighttime Allergy Relief", "product_id": "0135-1329_669165f1-6d53-4020-8f01-fbd9cb09c99b", "dosage_form": "TABLET", "product_ndc": "0135-1329", "generic_name": "triprolidine hcl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FLONASE", "brand_name_suffix": "Nighttime Allergy Relief", "active_ingredients": [{"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260228", "marketing_start_date": "20221215"}