Home NDC 73169-001 NO MORE NOSEBLEED
Product NDC 73169-001
11-digit product format 731690001
Labeler code 73169
Product ID 73169-001_ded8ef54-f9a3-4065-9d2d-fb7cb093926f
Type HUMAN OTC DRUG
Nonproprietary name Oxymetazoline Hydrochloride
Dosage form LIQUID
Route TOPICAL
Labeler DR. FRIEDMAN'S NO MORE NOSEBLEED KIT INC.
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-06-08
Substance OXYMETAZOLINE HYDROCHLORIDE
Active strength .05 g/100mL
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 NO MORE NOSEBLEED
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OXYMETAZOLINE HYDROCHLORIDE .05 g/100mL
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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73169-001-01 NO MORE NOSEBLEED 1 in 1 CARTON LIQUID 1 7 73169-001-01 NO MORE NOSEBLEED 30 mL in 1 BOTTLE, PLASTIC LIQUID 30 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73169-001 NO MORE NOSEBLEED (OXYMETAZOLINE HYDROCHLORIDE) LIQUID [DR. FRIEDMAN'S NO MORE NOSEBLEED KIT INC.] 6 Current NDC, Legacy NDC, 2 package rows 20241010_69d3f1fe-b476-4f84-8c5e-94957b74b46c.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 96 of 177 · 3,534 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 73169-001-01 73169000101 1 BOTTLE, PLASTIC in 1 CARTON (73169-001-01) / 30 mL in 1 BOTTLE, PLASTIC 2019-06-08 0000-00-00 No No Current