Label: SINUS RELIEF- kali bichromicum, luffa operculata, sabadilla spray
- NDC Code(s): 59262-240-20
- Packager: Similasan Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated April 26, 2021
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Uses*:
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Warnings:
- According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).
- Replace cap tightly after every use.
- To avoid contamination, do not touch the tip of the container to any surface besides nose.
- Discard open bottle after 6 months.
- The use of this container by more than one person may spread infection.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
- According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).
- Directions:
- Other information:
- Inactive Ingredients:
- Questions?
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INGREDIENTS AND APPEARANCE
SINUS RELIEF
kali bichromicum, luffa operculata, sabadilla sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59262-240 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 6 [hp_X] in 20 mL LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (LUFFA OPERCULATA FRUIT - UNII:C4MO6809HU) LUFFA OPERCULATA FRUIT 6 [hp_X] in 20 mL SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED 6 [hp_X] in 20 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59262-240-20 20 mL in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) 07/02/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/02/2013 Labeler - Similasan Corporation (111566530)