Nasal Solution

Manufacturer
Bullet Point LLC
Effective date
2026-01-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:32:58

Label at a glance#

ProductNasal Solution
Active ingredientPOVIDONE-IODINE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Povidone-lodine 1%

INACTIVE INGREDIENT SECTION

Purifed water,xylitol, vitamin D3,polysorbate, gellangum, carrageenan, sodiumhydroxide, aloe vera.

OTC - PURPOSE SECTION

*Gently washes and soothesthe delicate nasal passage.
*Helps clean away viruses,pollen, dust, and otherairborne contaminantsand germs.
Thins and loosens mucussecretion.
*Aids in improving airflow.
*Powerful sinus protection.
*Fast congestion relief.

INDICATIONS & USAGE SECTION

Uses:
*Congested nose andsinuses.
*lrritated and itchy nose.
*Nasal exposure to bacteria,dust and other airbornecontaminants.

OTC - DO NOT USE SECTION

Avoid use if you're allergicto iodine or inactive ingredient(s).Avoid contactin the eyes. Avoid use onchildren under 3 years old.

OTC - ASK DOCTOR SECTION

Stop use and consult adoctor if symptoms persistor worsen, swelling,infection, rash or feveroccurs.lf pregnant orbreast- feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach ofchildren. lf swallowed, getmedical help or contact the poison control center rightaway.

OTC - PREGNANCY OR BREAST FEEDING SECTION

lf pregnant orbreast- feeding, ask a health professional before use.

WARNINGS SECTION

Use of container bymore than one person canspread infection.

DOSAGE & ADMINISTRATION SECTION

Directions:
Adults and children over 6years of age: 1 spray in eachnostril not more than 3times in any 24-hour period,Children under é years ofage: Consult a doctor.
For the frst time -Removesafety seal and original capfrom bottle. insert dip tubeinto bottle, and screw on.
Gently blow your nose toclear the nasal passageway.Shake the product well,remove the cap, and thenspray it quickly and frmlyup your nostril.
Do not tilt your headbackward during sprayingAfter use, wipe the spraynozzle clean and securelyreattach the cap.

OTC - QUESTIONS SECTION

You can email us at support@noveha.com.com for more help!

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2675369povidone-iodine 1 % Nasal SprayPSN3
2675369povidone-iodine 10 MG/ML Nasal SpraySCD3
2675369povidone-iodine 1 % Nasal SpraySY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-135060643132099GTIN-13: 5060643132099
EAN-13: 5060643132099
GTIN storage (14 digits): 05060643132099
Nasal Spray Label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84008-101-01Nasal Solution30 mL in 1 BOTTLELIQUID303

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84008-10184008-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
4872ea4e-61d1-73c8-e063-6394a90a240f0e105e77-770b-d198-e063-6394a90a124f2026-01-01WarningsExact identifier
spl id: 4872ea4e-61d1-73c8-e063-6394a90a240f
spl set id: 0e105e77-770b-d198-e063-6394a90a124f

Reported adverse events (FAERS/openFDA)#

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