NEKVNRO ORIGINAL NASAL- naphazoline hcl 1%original nasal spray

Nekvnro ORIGINAL NASAL by

Drug Labeling and Warnings

Nekvnro ORIGINAL NASAL by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

NaphazolineHCL 1%

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

children under 2 years

When Using

·do not exceed recommended dosage
·do not use this product for more than 7 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 ofthis container by more than one person mayspread infection

Stop Use

symptoms persist.

Ask Doctor

children 2 to under 6 years.

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

do not exceed 25°C

Inactive ingredients

borneol, Camphorglycerin,Glycerol, menthol, propylene ,glycol, etc.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO ORIGINAL NASAL 
naphazoline hcl 1%original nasal spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV)	NAPHAZOLINE HYDROCHLORIDE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCEROL FORMAL (UNII: 3L7GR2604E)
MENTHOL (UNII: L7T10EIP3A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BORNEOL (UNII: M89NIB437X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-023-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/18/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	08/18/2024

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-023)