Label: BURBLE- sodium chloride tablet, for solution
- NDC Code(s): 83557-001-30
- Packager: LETS BURBLE, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Use
-
Warnings
- Prior to use read the detailed warnings and usage instruction for the Burble Nasal Irrigation Bottle included with the device or on our website at www.letsburble.com
- Use only Burble tablets in Burble Nasal Irrigation Bottle
- Do not use unfiltered tap water to dissolve tablets in Burble Nasal Irrigation bottle
- Other Infomation
- Directions
- Inactive Ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PDP
-
INGREDIENTS AND APPEARANCE
BURBLE
sodium chloride tablet, for solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83557-001 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 2860 mg CALCIUM BICARBONATE (UNII: 7PRA4BLM2L) (BICARBONATE ION - UNII:HN1ZRA3Q20) CALCIUM BICARBONATE 65 mg Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) POVIDONE K90 (UNII: RDH86HJV5Z) POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B) Product Characteristics Color white Score no score Shape ROUND Size 22mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83557-001-30 30 in 1 BAG; Type 1: Convenience Kit of Co-Package 05/08/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 05/08/2024 Labeler - LETS BURBLE, INC. (119182610)