CVS- sodium chloride, sodium bicarbonate kit

CVS by

Drug Labeling and Warnings

CVS by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

(in each packet)

Sodium Bicarbonate USP 700 mg

Sodium Chloride USP 2300 mg

PURPOSE

Purpose

Nasal Wash

INDICATIONS & USAGE

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

Warnings

Stop use and ask a doctor if washing is uncomfortable or

symptoms are not relieved

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
• Top rack of dishwasher safe
• Do not heat in microwave

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

• 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

See enclosed instruction sheet for complete directions and proper use

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 # and expiration date

INACTIVE INGREDIENT

Inactive ingredients

None

QUESTIONS

Questions?

1-888-547-5492

PATIENT PACKAGE INSERT

PATIENT PACKAGE INSERT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS 
sodium chloride, sodium bicarbonate kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-453

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-453-10	1 in 1 KIT	04/24/2017

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 PACKET	3000 mg
Part 2	1 CARTON	1

Part 1 of 2

CVS 
sodium bicarbonate, sodium chloride powder

Product Information
Item Code (Source)	NDC: 59779-408
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	22.8 mg  in 100 mg
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	77.8 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1		30 in 1 KIT
1	NDC: 59779-408-01	3000 mg in 1 PACKET; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/01/2013

Part 2 of 2

CVS SOFT TIP SQUEEZE BOTTLE 
applicator, ent

Product Information
Item Code (Source)	GS1:30707387763634

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	GS1:307073877636	1 in 1 CARTON; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
exempt device	KCJ

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/24/2017

Labeler - CVS Pharmacy (062312574)