Home NDC 13709-232 SinuFrin Plus
Product NDC 13709-232
11-digit product format 137090232
Labeler code 13709
Product ID 13709-232_0eb0fd3c-87e2-405d-e063-6294a90ae06f
Type HUMAN OTC DRUG
Nonproprietary name Oxymetazoline Hydrochloride
Dosage form SPRAY
Route NASAL
Labeler NeilMed Pharmaceuticals, Inc.
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-07-15
Substance OXYMETAZOLINE HYDROCHLORIDE
Active strength 7.5 mg/15mL
Pharmacologic classes Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 SinuFrin Plus
Brand name suffix NeilMed
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OXYMETAZOLINE HYDROCHLORIDE 7.5 mg/15mL
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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1000990 Internal RxNorm lookup 1313914 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 13709-232-05 SinuFrin PlusNeilMed 15 mL in 1 BOX SPRAY 15 9 13709-232-06 SinuFrin PlusNeilMed 15 mL in 1 BOTTLE SPRAY 15 9 13709-232-12 SinuFrin PlusNeilMed 1 in 1 CARTON SPRAY 1 9 13709-232-12 SinuFrin PlusNeilMed 30 mL in 1 BOTTLE SPRAY 30 9
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded OXYMETAZOLINE HYDROCHLORIDE ACTIVE INGREDIENT K89MJ0S5VY SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 OXYMETAZOLINE ACTIVE MOIETY 8VLN5B44ZY SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 ALLANTOIN INACTIVE INGREDIENT 344S277G0Z SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 ALOE INACTIVE INGREDIENT V5VD430YW9 SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 BENZALKONIUM CHLORIDE INACTIVE INGREDIENT F5UM2KM3W7 SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 SODIUM BICARBONATE INACTIVE INGREDIENT 8MDF5V39QO SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4 WATER INACTIVE INGREDIENT 059QF0KO0R SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 13709-232 SINUFRIN PLUS NEILMED (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [NEILMED PHARMACEUTICALS, INC.] 9 Current NDC, Legacy NDC, 4 package rows 20240112_99afe6a6-1350-49c6-9347-b7e531e35925.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 13709-232-05 13709023205 15 mL in 1 BOX (13709-232-05) 15 ml 2012-07-15 0000-00-00 No No Current 13709-232-06 13709023206 15 mL in 1 BOTTLE (13709-232-06) 15 ml 2012-07-15 0000-00-00 No No Current 13709-232-12 13709023212 1 BOTTLE in 1 CARTON (13709-232-12) / 30 mL in 1 BOTTLE 1 bottle 2021-04-21 0000-00-00 No No Current