Home NDC 33992-8684 ASSURED NASAL RELIEF ORIGINAL
Product NDC 33992-8684
11-digit product format 339928684
Labeler code 33992
Product ID 33992-8684_db88efcb-e172-5f71-e053-2a95a90a0be1
Type HUMAN OTC DRUG
Nonproprietary name OXYMETAZOLINE HYDROCHLORIDE
Dosage form SPRAY
Route NASAL
Labeler GREENBRIER INTERNATIONAL, INC.
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2011-03-08
Marketing end 0000-00-00
Substance OXYMETAZOLINE HYDROCHLORIDE
Active strength 0 g/100mL
Pharmacologic classes Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 33992-8684-5 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 33992-8684-5 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 33992-8684-5 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 33992-8684-5 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 33992-8684-5 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 33992-8684-5 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 33992-8684-5 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 33992-8684-5 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 33992-8684-5 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 33992-8684-5 ASSURED NASAL RELIEF ORIGINAL 30 mL in 1 BOTTLE SPRAY 30 8 33992-8684-5 ASSURED NASAL RELIEF ORIGINAL 1 in 1 CARTON SPRAY 1 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded OXYMETAZOLINE HYDROCHLORIDE ACTIVE INGREDIENT K89MJ0S5VY ASSURED NASAL RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [GREENBRIER INTERNATIONAL, INC.] 2 OXYMETAZOLINE ACTIVE MOIETY 8VLN5B44ZY ASSURED NASAL RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [GREENBRIER INTERNATIONAL, INC.] 2 BENZALKONIUM CHLORIDE INACTIVE INGREDIENT F5UM2KM3W7 ASSURED NASAL RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [GREENBRIER INTERNATIONAL, INC.] 2 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K ASSURED NASAL RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [GREENBRIER INTERNATIONAL, INC.] 2 POLYETHYLENE GLYCOL INACTIVE INGREDIENT 3WJQ0SDW1A ASSURED NASAL RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [GREENBRIER INTERNATIONAL, INC.] 2 SODIUM PHOSPHATE, DIBASIC INACTIVE INGREDIENT GR686LBA74 ASSURED NASAL RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [GREENBRIER INTERNATIONAL, INC.] 2 SODIUM PHOSPHATE, MONOBASIC INACTIVE INGREDIENT 3980JIH2SW ASSURED NASAL RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [GREENBRIER INTERNATIONAL, INC.] 2 WATER INACTIVE INGREDIENT 059QF0KO0R ASSURED NASAL RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [GREENBRIER INTERNATIONAL, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 33992-8684 ASSURED NASAL RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [GREENBRIER INTERNATIONAL, INC.] 8 Legacy NDC, 2 package rows 20220401_5c86c949-fa0b-413d-9934-d4edb58ece8b.zip
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 33992-8684-5 33992868405 1 BOTTLE in 1 CARTON (33992-8684-5) > 30 mL in 1 BOTTLE 1 bottle 2016-11-07 0000-00-00 No No Current