Home NDC 82706-034 AXIV Sinus OVERNIGHT
Product NDC 82706-034
11-digit product format 827060034
Labeler code 82706
Product ID 82706-034_54f040c7-d89f-8b10-e063-6394a90aa0bf
Type HUMAN OTC DRUG
Nonproprietary name Oxymetazoline hydrochloride.
Dosage form SPRAY
Route NASAL
Labeler VIVUNT PHARMA LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-19
Substance OXYMETAZOLINE HYDROCHLORIDE
Active strength .5 mg/mL
Pharmacologic classes Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [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 AXIV Sinus OVERNIGHT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OXYMETAZOLINE HYDROCHLORIDE .5 mg/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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1000990 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 Sample Exclude flag Status 82706-034-01 82706003401 1 BOTTLE, SPRAY in 1 CARTON (82706-034-01) / 15 mL in 1 BOTTLE, SPRAY 2026-06-22 No No Current