FDA.reportPublic FDA data

Extra Moisturizing No Drip Nasal

Manufacturer
Walgreens | Product Quest Mfg.
Effective date
2018-02-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:54:33

Label at a glance#

ProductExtra Moisturizing 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.

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.

Warning

WARNINGS SECTION

Ask doctor before us 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. If symptoms persist, consult a doctor.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.

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
Glycerin
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 SprayPSN3
1000990oxymetazoline hydrochloride 0.5 MG/ML Nasal SpraySCD3
1000990oxymetazoline hydrochloride 0.05 % Nasal SpraySY3

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
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-7004-012020-01-31C16284748780-19d75b9d0-958c-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-7004-01Extra Moisturizing No Drip NasalWalgreens15 mL in 1 BOTTLELIQUID153
0363-7004-01Extra Moisturizing No Drip NasalWalgreens1 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-7004EXTRA MOISTURIZING NO DRIP NASAL WALGREENS (OXYMETAZOLINE HYDROCHLORIDE - 0.05%) LIQUID [WALGREENS]3Legacy NDC, 2 package rows20180215_0fc2571f-dc1a-4e22-b4fe-d8094bcde3d9.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-70040363-7004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
Oxymetazoline HydrochlorideK89MJ0S5VYACTIB
Benzalkonium ChlorideF5UM2KM3W7IACT
Benzyl AlcoholLKG8494WBHIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORMK679OBS311IACT
EDETATE DISODIUM7FLD91C86KIACT
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS22ADO53M6FIACT
GlycerinPDC6A3C0OXIACT
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
77df9152-a348-40a4-b3c1-cfc81f998b0f0fc2571f-dc1a-4e22-b4fe-d8094bcde3d92018-02-14WarningsExact identifier
spl id: 77df9152-a348-40a4-b3c1-cfc81f998b0f
spl set id: 0fc2571f-dc1a-4e22-b4fe-d8094bcde3d9

Reported adverse events (FAERS/openFDA)#

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