NATUHEAL ORIGINAL NASAL- naphazoline hcl 0.05% original nasal spray

NATUHEAL ORIGINAL NASAL by

Drug Labeling and Warnings

NATUHEAL ORIGINAL NASAL by is a Otc medication manufactured, distributed, or labeled by Jiangxi Yudexi Pharmaceutical Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Naphazoline HCL 0.05%.

Purpose

Nasal Decongestant

Use

temporarily relieves ·nasal congestion due to a cold, hay fever, or other upper respiratory allergies ·sinus congestion and pressure

Warnings

Ask a doctor before use if you have ·heart disease ·high blood pressure
.thyroid disease ·diabetes ·trouble urinating due to enlarged prostate gland

Do not use

·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 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

When Using

·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 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

Stop Use

Stop use and ask a doctor if symptoms persist.

Ask Doctor

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

Keep Oot Of Reach Of Children

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

Directions

adults&children 6 yrs &older(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 24 hours

Other information

Store at 20° to 25°C(68° to 77°F)

Inactive ingredients

borneol,Camphor,glycerin,menthol，propylene glycol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NATUHEAL ORIGINAL NASAL 
naphazoline hcl 0.05% original nasal spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-083
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NAPHAZOLINE HCL (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV)	NAPHAZOLINE HCL	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
MENTHOL (UNII: L7T10EIP3A)
BORNEOL (UNII: M89NIB437X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-083-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	02/08/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)