Label: SOFT TIP SQUEEZE BOTTLE SINUS WASH MEIJER- sodium bicarbonate, sodium chloride kit
- NDC Code(s): 42829-998-00, 79481-0501-1
- Packager: Meijer, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 17, 2024
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- PURPOSE
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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- DOSAGE & ADMINISTRATION
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- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
SOFT TIP SQUEEZE BOTTLE SINUS WASH MEIJER
sodium bicarbonate, sodium chloride kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-0501 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79481-0501-1 1 in 1 KIT; Type 1: Convenience Kit of Co-Package 01/09/2022 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 30 PACKET 90000 mg Part 1 of 1 SINUS WASH SALINE REFILLS
sodium bicarbonate, sodium chloride powder, for solutionProduct Information Item Code (Source) NDC:42829-998 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 2300 mg in 3000 mg SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37, BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE 700 mg in 3000 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42829-998-00 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 01/09/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/09/2022 Labeler - Meijer, Inc. (006959555)