Label: INCARVEXX ESSENTIAL- sodium chloride, iodine spray
- NDC Code(s): 80897-030-35
- Packager: Nobu Baby LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 10, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- Uses
- Directions
- KEEP OUT OF REACH OF CHILDREN
- Warnings
- INACTIVE INGREDIENT
- Other information or comments
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
INCARVEXX ESSENTIAL
sodium chloride, iodine sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80897-030 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 20 ug in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 9 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:80897-030-35 1 in 1 CARTON 06/22/2021 1 35 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/22/2021 Labeler - Nobu Baby LLC (090064974) Establishment Name Address ID/FEI Business Operations STERGIOULAS, STYLIANOS, & CO. E.E. "PHARMACOSMETIC - DIAFARM" 499700727 manufacture(80897-030)