SKAPEMED ORIGINAL NASAL

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2025-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:40:39

Label at a glance#

ProductSKAPEMED ORIGINAL NASAL
Active ingredientNAPHAZOLINE HCL
Label structure13 sections

Dosage and administration

Adults&children 6 years &older(with adult supervision ): 2 or 3 sprays in eachnostril, not more often than every 10 to 12 hours.Do not exceed 2 doses in 24 hours

Storage and handling

do not exceed 25°C. Retain the box for future reference on fulllabeling.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Naphazoline HCL 0.05%.

Purpose

OTC - PURPOSE SECTION

Nasal Decongestant

Use

INDICATIONS & USAGE SECTION

temporarily relieves

·Nasal congestion due to a cold, hay fever, or other upper respiratory allergies

·Sinus congestion and pressure

Warnings

WARNINGS SECTION

1.Do not use if you are allergic to the ingredients,
2.Ask a doctor before use if you have
Heart disease、High blood pressure、Thyroid disease、Diabetes、Trouble urinating
due to enlarged prostate gland
3.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 prolongeduse may cause nasal congestion to recur or worsen.

·Temporary discomfort such as burning,stinging,sneezing,or increased nasal discharge may occur.

·Use of this container by more than one person may spread infection.

Do not use

OTC - DO NOT USE SECTION

children under 2 years.Shake well before use. Before using the first time.remove the protective cap & safely clip from the tip and prime metered pump by depressing firmly several times. To spray, hold bottle with thumb at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostril. Fully depress pump all the way down with a firm even stroke and sniff deeply. Wipe nozzle clean after use.

When Using

OTC - WHEN USING SECTION

·Do not exceed recommended dosage

· Do not use this product for more than 3 days.Use only as directed. Frequent or prolongeduse may cause nasal congestion to recur or worsen.

·Temporary discomfort such as burning,stinging,sneezing,or increased nasaldischarge may occur.

·Use of this container by more than one person may spread infection.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist.

Ask Doctor

OTC - ASK DOCTOR SECTION

children 2 to under 6 years.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed,get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Adults&children 6 years &older(with adult supervision ): 2 or 3 sprays in eachnostril, not more often than every 10 to 12 hours.Do not exceed 2 doses in 24 hours

Other information

STORAGE AND HANDLING SECTION

do not exceed 25°C. Retain the box for future reference on fulllabeling.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Borneol,Camphor,glycerin,propylene glycol.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136974603692587GTIN-13: 6974603692587
EAN-13: 6974603692587
GTIN storage (14 digits): 06974603692587
Label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e18001c8-33ae-5f66-9cdc-a39724bd4573Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84010-05584010-055-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
4a47448a-b29f-fbb6-e063-6294a90a120829976f90-37be-d605-e063-6294a90a7fc72026-02-07WarningsExact identifier
spl set id: 29976f90-37be-d605-e063-6294a90a7fc7

Reported adverse events (FAERS/openFDA)#

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