Home NDC 69842-648 Nasal
Product NDC 69842-648
11-digit product format 698420648
Labeler code 69842
Product ID 69842-648_6a23d1cb-817f-47ef-9fbe-368c18589b28
Type HUMAN OTC DRUG
Nonproprietary name Phenylephrine hydrochloride
Dosage form SPRAY
Route NASAL
Labeler CVS Pharmacy
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-06-25
Substance PHENYLEPHRINE HYDROCHLORIDE
Active strength 1 g/100mL
Pharmacologic classes Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
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
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENYLEPHRINE HYDROCHLORIDE 1 g/100mL
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 1087043 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 69842-648-10 Nasal 1 in 1 CARTON SPRAY 1 4 69842-648-10 Nasal 30 mL in 1 BOTTLE, SPRAY SPRAY 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-648 NASAL (PHENYLEPHRINE HYDROCHLORIDE) SPRAY [CVS PHARMACY] 4 Current NDC, Legacy NDC, 2 package rows 20241105_694a3116-1b75-42cd-bbcf-d19831c2d796.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 73 of 178 · 3,551 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 69842-648-10 69842064810 1 BOTTLE, SPRAY in 1 CARTON (69842-648-10) / 30 mL in 1 BOTTLE, SPRAY 2018-06-25 0000-00-00 No No Current