Label: GURUNANDA NASAL SALINE- nasal wash powder, for solution
- NDC Code(s): 70708-210-08
- Packager: GURUNANDA LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 26, 2024
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
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Uses
- Restores vital moisture to provide prompt relief for dry , crusted and inflamed nasal membranes due to chronic sinusitis,colds , low humidity, overuse of nasal decongestant drops and sprays, allergies, minor nose bleeds and other minor nasal irritations.
- Temporarily relieves nasal stuffiness.
- Reduces swelling of nasal passages; shrinks swollen membranes.
- Promotes nasal and/or sinus drainage; temporarily relieves sinus congestion and pressure.
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other Information
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GURUNANDA NASAL SALINE
nasal wash powder, for solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70708-210 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE 0.515 g in 2.2 g SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 1.685 g in 2.2 g Product Characteristics Color white (WHITE CRYSTALLINE GRANULE POWDER) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70708-210-08 8 in 1 BOX 02/12/2024 1 2.2 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/12/2024 Labeler - GURUNANDA LLC (079671169)