nasal decongestant pe non-drowsy maximum strength

Generic: phenylephrine hcl

Labeler: chain drug marketing association inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name nasal decongestant pe non-drowsy maximum strength
Generic Name phenylephrine hcl
Labeler chain drug marketing association inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

phenylephrine hydrochloride 10 mg/1

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION INC

Identifiers & Regulatory

Product NDC 63868-144
Product ID 63868-144_d534021e-9167-4966-bd79-d13ee792282b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2005-01-14
Marketing End 2027-11-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868144
Hyphenated Format 63868-144

Supplemental Identifiers

RxCUI
1049182
UPC
0635515954991
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 non-drowsy 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 (63868-144-19) / 18 TABLET, FILM COATED in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (63868-144-37) / 18 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (2)

63868-144-19 1 BLISTER PACK in 1 CARTON (63868-144-19) / 18 TABLET, FILM COATED in 1 BLISTER PACK 63868-144-37 2 BLISTER PACK in 1 CARTON (63868-144-37) / 18 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

phenylephrine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Nasal Decongestant PE Non-Drowsy Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d534021e-9167-4966-bd79-d13ee792282b", "openfda": {"upc": ["0635515954991"], "unii": ["04JA59TNSJ"], "rxcui": ["1049182"], "spl_set_id": ["bf7246c1-90fe-4de8-8bb2-e5ff7e8ca63d"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63868-144-19)  / 18 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "63868-144-19", "marketing_end_date": "20270731", "marketing_start_date": "20050114"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63868-144-37)  / 18 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "63868-144-37", "marketing_end_date": "20271130", "marketing_start_date": "20050114"}], "brand_name": "Nasal Decongestant PE Non-Drowsy Maximum Strength", "product_id": "63868-144_d534021e-9167-4966-bd79-d13ee792282b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "63868-144", "generic_name": "Phenylephrine HCl", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nasal Decongestant PE", "brand_name_suffix": "Non-Drowsy Maximum Strength", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20271130", "marketing_start_date": "20050114"}