No Drip Nasal Spray

Manufacturer
NeilMed Pharmaceuticals Inc
Effective date
2026-08-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-08-08 02:01:17

Label at a glance#

ProductNo Drip
Active ingredientOXYMETAZOLINE HYDROCHLORIDE
Label structure13 sections

Indications and uses

■ Temporarily relieves nasal congestion due to: ■ Common cold ■ Hay fever ■ Upper respiratory allergies ■ Temporarily relieves sinus congestion and pressure ■ Shrinks swollen nasal membranes so you can breathe more freely

Dosage and administration

■ 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: ask a doctor To Use: Push firmly down on cap and turn counter clockwise. To spray, squeeze bottle quickly and firmly. Do not tilt head backward while spraying. Wipe nozzle clean after use. Sec...

Storage and handling

■ Store between 68° F (20° C) and 86° F (30° C) ■ Retain carton for future reference on full labeling

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Oxymetazoline hydrochloride 0.05%. Active IngredientActive Ingredient

Purpose

OTC - PURPOSE SECTION

Nasal Decongestant PurposePurpose

Uses

INDICATIONS & USAGE SECTION


■ Temporarily relieves nasal congestion due to:
■ Common cold
■ Hay fever
■ Upper respiratory allergies
■ Temporarily relieves sinus congestion and
pressure
■ Shrinks swollen nasal membranes so you can
breathe more freely Indications and UsesIndications and Uses

Warnings

WARNINGS SECTION

Ask a doctor before use if you have
■ Heart disease ■ High blood pressure
■ Diabetes ■ Thyroid disease
■ Trouble urinating due to an enlarged prostate
gland WarningsWarnings

When using this product

OTC - WHEN USING SECTION

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

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist Stop use and ask a doctor ifStop use and ask a doctor if

pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use. pregnancy or breast feedingpregnancy or breast feeding

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222). Keep out of reach of children.Keep out of reach of children.

Directions

INSTRUCTIONS FOR USE 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: ask a doctor To Use: Push firmly down on cap and turn counter clockwise. To spray, squeeze bottle quickly and firmly. Do not tilt head backward while spraying. Wipe nozzle clean after use. Secure cap after use. Instructions For UseInstructions For Use

Other Information

STORAGE AND HANDLING SECTION

■ Store between 68° F (20° C) and 86° F (30° C)
■ Retain carton for future reference on full labeling storagestorage

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sodium chloride, sodium bicarbonate, propylene glycol, edetate disodium, benzalkonium chloride, purified water. Inactive IngredientsInactive Ingredients

How to use:

DOSAGE & ADMINISTRATION SECTION


Hold white tabs, SQUEEZE grooved areaofcap FIRMLY and turn counter clockwise. Secure cap after use.

Directions
■ 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. Dosage and AdministrationDosage and Administration

No Drip Nasal Spray

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

Packaging label principal display panelsPackaging label principal display panels

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130705928700109GTIN-13: 0705928700109
EAN-13: 0705928700109
GTIN-12: 705928700109
UPC-A: 705928700109
GTIN storage (14 digits): 00705928700109
2850-TGT-US-Rev4_page-0001.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e67be450-f8e4-4bc1-88bd-1259d379f55fProduct name120210127
c53f3286-4062-4cf5-8355-399519c639a6Product name120170424
a993dfc5-f219-4460-bde6-30dd724d9ef0Product name120160818

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
13709-31513709-315-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-01-11full-release2026-06-01 00:07:05

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
No DripOXYMETAZOLINE HYDROCHLORIDENeilMed Pharmaceuticals Ince9b799ad-9164-7f30-e053-2a95a90a00c52026-08-05WarningsExact identifier
ndc (package): 13709-315-01
ndc (product): 13709-315
ndc11 (package): 13709031501
spl id: 584d11a5-22c2-6bde-e063-6294a90a073c
spl set id: e9b799ad-9164-7f30-e053-2a95a90a00c5

Reported adverse events (FAERS/openFDA)#

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