Home NDC 64336-015 Vicks Sinex SEVERE
Product NDC 64336-015
11-digit product format 643360015
Labeler code 64336
Product ID 64336-015_500f4bf5-d18d-d334-e063-6394a90a16fd
Type HUMAN OTC DRUG
Nonproprietary name Oxymetazoline Hydrochloride
Dosage form SPRAY
Route NASAL
Labeler Procter & Gamble Manufacturing GmbH
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-07-10
Marketing end 2028-02-28
Substance OXYMETAZOLINE HYDROCHLORIDE
Active strength .05 g/mL
Pharmacologic classes Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [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 Vicks Sinex SEVERE
Brand name suffix MOISTURIZING ULTRA FINE MIST Active Ingredients# Ingredient, Strength table Ingredient Strength OXYMETAZOLINE HYDROCHLORIDE .05 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K89MJ0S5VY Internal UNII 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 64336-015-01 Vicks Sinex SEVEREMOISTURIZING ULTRA FINE MIST 1 in 1 CARTON SPRAY 1 8 64336-015-01 Vicks Sinex SEVEREMOISTURIZING ULTRA FINE MIST 15 mL in 1 BOTTLE, PUMP SPRAY 15 8 64336-015-02 Vicks Sinex SEVEREMOISTURIZING ULTRA FINE MIST 15 mL in 1 BOTTLE, PUMP SPRAY 15 8 64336-015-02 Vicks Sinex SEVEREMOISTURIZING ULTRA FINE MIST 2 in 1 CARTON SPRAY 2 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64336-015 VICKS SINEX SEVERE MOISTURIZING ULTRA FINE MIST (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [PROCTER & GAMBLE MANUFACTURING GMBH] 6 Current NDC, 4 package rows 20241012_f4b01827-7444-3bfc-e053-2a95a90aebed.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 64336-015-01 64336001501 1 BOTTLE, PUMP in 1 CARTON (64336-015-01) / 15 mL in 1 BOTTLE, PUMP 2018-07-10 2028-02-28 No No Historical 64336-015-02 64336001502 2 BOTTLE, PUMP in 1 CARTON (64336-015-02) / 15 mL in 1 BOTTLE, PUMP 2024-07-09 2028-02-28 No No Historical