CVS Sinus Wash

Manufacturer
Denison Pharmaceuticals, LLC
Effective date
2019-02-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:29:21

Label at a glance#

ProductCVS Sinus Wash
Active ingredientSODIUM CHLORIDE, SODIUM BICARBONATE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

(in each prefilled bottle)

Sodium Bicarbonate USP 700 mg

Sodium Chloride USP 2300 mg

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

(in each packet)

Sodium Bicarbonate USP 700 mg

Sodium Chloride USP 2300 mg

OTC - PURPOSE SECTION

Purpose

Nasal Wash

OTC - PURPOSE SECTION

Purpose

Nasal Wash

INDICATIONS & USAGE SECTION

Uses

Temporarily relieves symptoms associated with

sinusitis, cold, flu or allergies:

-Sneezing

-Runny nose

-Nasal stuffiness

-Post nasal drip

-Removes inhaled irritants (dust, pollen)

-Promotes nasal and sinus drainage

-Helps reduce swelling of nasal membranes

-Moisturizes dry nasal passages

WARNINGS SECTION

Warnings

Stop use and ask a doctor if washing is uncomfortable or

symptoms are not reduced.

Do not use unfiltered tap water. See instructions inside box

for proper water sources.

Do not use if nasal passages are completely blocked or if you

have an ear infection or blocked ears.

When using this product:

  • Use by only one person
  • Wash with soap and water after each use
  • Do not heat in microwave

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Directions:

Adults and children 4 years and over:  use 1  -  2 packets per 8 fl. oz (240 mL) up to every 2 hours as needed

Children under 4 years:  Consult a physician

Prior to first use see enclosed instruction sheet for complete directions

OTHER SAFETY INFORMATION

Other information

  • Inspect saline packets for integrity
  • Do not use saline packets if open or torn
  • Protect saline packets from excessive heat and moisture
  • See saline packets or box for lot no. and expiration date

INACTIVE INGREDIENT SECTION

Inactive ingredients

(in each prefilled bottle)

Purified Water USP, Benzalkonium Chloride USP (Preservative)

Inactive ingredients

(in each packet)

None

OTC - QUESTIONS SECTION

Questions?

1-888-547-5492

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0295-48070295-4807-28

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

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
0780546f-282f-ae19-e063-6294a90abf0c82837451-6dab-2197-e053-2991aa0aa80a2023-10-12WarningsExact identifier
spl set id: 82837451-6dab-2197-e053-2991aa0aa80a

Reported adverse events (FAERS/openFDA)#

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