Label: WILD HORSE 777 MOISTURIZING NASAL- sodium chloride liquid
- NDC Code(s): 80771-000-15
- Packager: Wild Horse 777, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated March 14, 2022
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient:
- Uses
- Warnings
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Directions
- 12 years old - adult:3 sprays in each nostril.
- 6-12 years old: 2 sprays in each nostril.
- 2-6 years old: 1 spray in each nostril.
- Children under age 2:1 spray. Consult a physician.
- User should be in an upright position.
- Remove cap, insert the nozzle into the nostril and depress the pump completely while sniffing deeply.
- Day 1: every 3-4 hours.
- Day 2: every 3-4 hours.
- Day 3: twice a day.
- Day 4: at bedtime.
- Day 5: at bedtime.
- Day 6-9: skip.
- Day 10: at bedtime (final dose).
- Other Information
- Inactive Ingredient:
- Questions and Comments:
- Package Labeling:
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INGREDIENTS AND APPEARANCE
WILD HORSE 777 MOISTURIZING NASAL
sodium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80771-000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 6.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80771-000-15 1 in 1 BOX 10/02/2020 1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/02/2020 Labeler - Wild Horse 777, Inc. (117632276)