Home NDC 67091-207 Nasal Decongestant PE
Product NDC 67091-207
11-digit product format 670910207
Labeler code 67091
Product ID 67091-207_55ddbcde-7c68-43cd-8816-7b75ec04ccec
Type HUMAN OTC DRUG
Nonproprietary name Phenylephrine HCl
Dosage form TABLET, FILM COATED
Route ORAL
Labeler WinCo Foods, LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-01-14
Marketing end 2026-11-15
Substance PHENYLEPHRINE HYDROCHLORIDE
Active strength 10 mg/1
Pharmacologic classes Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag No
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Nasal Decongestant PE
Brand name suffix Maximum Strength Active Ingredients# Ingredient, Strength table Ingredient Strength PHENYLEPHRINE HYDROCHLORIDE 10 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 04JA59TNSJ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1049182 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67091-207-18 Nasal Decongestant PEMaximum Strength 1 in 1 CARTON TABLET, FILM COATED 1 17 67091-207-18 Nasal Decongestant PEMaximum Strength 18 in 1 BLISTER PACK TABLET, FILM COATED 18 17 67091-207-72 Nasal Decongestant PEMaximum Strength 3 in 1 CARTON TABLET, FILM COATED 3 17 67091-207-72 Nasal Decongestant PEMaximum Strength 24 in 1 BLISTER PACK TABLET, FILM COATED 24 17
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded PHENYLEPHRINE HYDROCHLORIDE ACTIVE INGREDIENT 04JA59TNSJ NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 PHENYLEPHRINE ACTIVE MOIETY 1WS297W6MV NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 DEXTROSE MONOHYDRATE INACTIVE INGREDIENT LX22YL083G NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 SODIUM CITRATE INACTIVE INGREDIENT 1Q73Q2JULR NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET [WINCO FOODS, LLC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67091-207 NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET, FILM COATED [WINCO FOODS, LLC] 17 Current NDC, Legacy NDC, 4 package rows 20250108_bb7a9fed-dc04-4c31-aa7f-4185d955242c.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 74 of 180 · 3,583 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 67091-207-18 67091020718 1 BLISTER PACK in 1 CARTON (67091-207-18) / 18 TABLET, FILM COATED in 1 BLISTER PACK 1 blister pack 2005-01-14 2026-11-15 No No Current 67091-207-72 67091020772 3 BLISTER PACK in 1 CARTON (67091-207-72) > 24 TABLET, FILM COATED in 1 BLISTER PACK 3 blister pack 2005-01-14 0000-00-00 No No Current