FDA.reportPublic FDA data

Original No Drip Nasal

Manufacturer
Walgreens | Product Quest Mfg.
Effective date
2018-01-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:54:01

Label at a glance#

ProductOriginal No Drip Nasal Walgreens
Active ingredientOxymetazoline Hydrochloride
Label structure6 sections

Indications and uses

For the temporary relief of nasal congestion due to the common cold, hay fever or other upper respiratory allergies. Shrinks swollowen membranes so you can breathe more freely

Label contents#

Full prescribing information#

Active ingredient                                  Purpose

OTC - ACTIVE INGREDIENT SECTION

Oxymetazoline Hydrochloride - 0.05% Nazal Decongestant

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of nasal congestion due to the common cold, hay fever or other upper respiratory allergies. Shrinks swollowen membranes so you can breathe more freely

Warnings

WARNINGS SECTION

Ask doctor before use if person has heart disease, high blood pressure, thyroid disease, diabetes, or if adult has difficulty in urination due to enlargement of the prostate gland unless directed by a doctor.

When using this product

Do not exceed recommended dosage

Do not use this product for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen. This product may cause temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge. The use of this container by more than one person may spread infection.

​Stop Use and ask doctor if symptoms persist

Direction

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period. Children under 6 years of age: consult a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium Chloride
Benzyl Alcohol
Cellulose Gum
Disodium EDTA
Disodium Phosphate
Flavor
Microcrystalline Cellulose
PEG-12
Povidone
Sodium Phosphate
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1000990oxymetazoline HCl 0.05 % Nasal SprayPSN4
1000990oxymetazoline hydrochloride 0.5 MG/ML Nasal SpraySCD4
1000990oxymetazoline hydrochloride 0.05 % Nasal SpraySY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
OXYMETAZOLINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
e67be450-f8e4-4bc1-88bd-1259d379f55fProduct name120210127
c53f3286-4062-4cf5-8355-399519c639a6Product name120170424
a993dfc5-f219-4460-bde6-30dd724d9ef0Product name120160818
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-7005-012020-01-31C16284748780-19d75b9d0-f43f-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-7005-01Original No Drip NasalWalgreens1 in 1 CARTONLIQUID14
0363-7005-01Original No Drip NasalWalgreens15 mL in 1 BOTTLELIQUID154

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-7005ORIGINAL NO DRIP NASAL WALGREENS (OXYMETAZOLINE HYDROCHLORIDE - 0.05%) LIQUID [WALGREENS]4Legacy NDC, 2 package rows20180108_83e2eaf3-c3aa-47c6-88da-78ec0fee3b01.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-7005-01ML - Milliliter0363-7005ee32fb77-f902-47f1-a6c9-7cdc938906fe12022-06-06

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-70050363-7005-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
Oxymetazoline HydrochlorideK89MJ0S5VYACTIB
Benzalkonium ChlorideF5UM2KM3W7IACT
Benzyl AlcoholLKG8494WBHIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS22ADO53M6FIACT
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT
POLYETHYLENE GLYCOL 600NL4J9F21N9IACT
PovidoneFZ989GH94EIACT
Sodium PhosphateSE337SVY37IACT
water059QF0KO0RIACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6684bb5e-ecfc-433d-84c6-26c7cb469d8c83e2eaf3-c3aa-47c6-88da-78ec0fee3b012018-01-08WarningsExact identifier
spl id: 6684bb5e-ecfc-433d-84c6-26c7cb469d8c
spl set id: 83e2eaf3-c3aa-47c6-88da-78ec0fee3b01

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.