Label: CVS- sodium chloride, sodium bicarbonate kit
- NDC Code(s): 69842-324-01, 69842-453-10
- Packager: CVS Pharmacy, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
Warnings
• Stop use and ask a doctor ifwashing 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 blockedor 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
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PATIENT PACKAGE INSERT
- PATIENT PACKAGE INSERT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CVS
sodium chloride, sodium bicarbonate kitProduct 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 1 of 1 CVS
sodium bicarbonate, sodium chloride powderProduct Information Item Code (Source) NDC:69842-324 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) 77.8 mg in 100 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 30 in 1 KIT 1 NDC:69842-324-01 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 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/24/2017 Labeler - CVS Pharmacy, Inc. (062312574)