nasal decongestant pe maximum strength

Generic: phenylephrine hcl

Labeler: cardinal health 110, llc. dba leader
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name nasal decongestant pe maximum strength
Generic Name phenylephrine hcl
Labeler cardinal health 110, llc. dba leader
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

phenylephrine hydrochloride 10 mg/1

Manufacturer
Cardinal Health 110, LLC. DBA Leader

Identifiers & Regulatory

Product NDC 70000-0126
Product ID 70000-0126_5217c596-a8d8-4474-bd8a-befc867afd43
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2005-01-14
Marketing End 2026-03-31

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 700000126
Hyphenated Format 70000-0126

Supplemental Identifiers

RxCUI
1049182
UPC
0096295129496
UNII
04JA59TNSJ

Packaging Origin

Original Packager
true

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 nasal decongestant pe maximum strength (source: ndc)
Generic Name phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (70000-0126-1) / 18 TABLET, FILM COATED in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (70000-0126-2) / 24 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (2)

70000-0126-1 1 BLISTER PACK in 1 CARTON (70000-0126-1) / 18 TABLET, FILM COATED in 1 BLISTER PACK 70000-0126-2 3 BLISTER PACK in 1 CARTON (70000-0126-2) / 24 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

phenylephrine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Nasal Decongestant PE Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5217c596-a8d8-4474-bd8a-befc867afd43", "openfda": {"upc": ["0096295129496"], "unii": ["04JA59TNSJ"], "rxcui": ["1049182"], "spl_set_id": ["0e804d71-1a61-4131-9b00-fde3ada7c7f8"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (70000-0126-1)  / 18 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70000-0126-1", "marketing_end_date": "20260331", "marketing_start_date": "20050114"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70000-0126-2)  / 24 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70000-0126-2", "marketing_end_date": "20260331", "marketing_start_date": "20050114"}], "brand_name": "Nasal Decongestant PE Maximum Strength", "product_id": "70000-0126_5217c596-a8d8-4474-bd8a-befc867afd43", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "70000-0126", "generic_name": "Phenylephrine HCl", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nasal Decongestant PE", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260331", "marketing_start_date": "20050114"}