País: Estats Units
Idioma: anglès
Font: NLM (National Library of Medicine)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6), POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V)
EMS Contract Packaging
EUCALYPTUS GLOBULUS LEAF
EUCALYPTUS GLOBULUS LEAF 20 [hp_X] in 100 mL
TOPICAL
OTC DRUG
PURPOSE ANTISEPTIC RELIEVES SINUS PAIN, PRESSURE AND INFLAMMATION USES RELIEVES NASAL AND SINUS SYMPTOMS ASSOCIATED WITH PERSISTENT SINUS CONDITIONS: - CONGESTION - NASAL INFLAMMATION - SINUS PRESSURE - FACIAL PIN - SINUS HEADACHE - STUFFY NOSE
unapproved drug other
SINOFRESH NASAL AND SINUS CARE- EUCALYPTUS GLOBULUS LEAF, POTASSIUM DICHROMATE LIQUID EMS CONTRACT PACKAGING _Disclaimer: This drug has not been found by FDA to be safe and effective, and this_ _labeling has not been approved by FDA. For further information about unapproved_ _drugs, click here._ ---------- EMS (AS CMO) - SINOFRESH, NASAL (59228-103) ACTIVE INGREDIENTS EUCALYPTUS GLOBULUS 20X KALIUM BICHROMICUM 30X PURPOSE ANTISEPTIC RELIEVES SINUS PAIN, PRESSURE AND INFLAMMATION USES RELIEVES NASAL AND SINUS SYMPTOMS ASSOCIATED WITH PERSISTENT SINUS CONDITIONS: CONGESTION NASAL INFLAMMATION SINUS PRESSURE FACIAL PIN SINUS HEADACHE STUFFY NOSE ASK A DOCTOR BEFORE USE IF YOU HAVE HAD ANY MEDICAL PROCEDURES FOR YOUR NOSE OR SINUSES A BLEEDING OR IRRITATED NOSE KEEP OUT OF REACH OF CHILDREN. IF MORE THAN USED FOR SPRAYING IS ACCIDENTALLY SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY. DIRECTIONS ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER (WITH ADULT SUPERVISION) MORNING AND EVENING, APPLY 1 TO 2 SPRAYS TO EACH NOSTRIL. OTHER INGREDIENTS BENZALKONIUM CHLORIDE, CETYLPYRIDINIUM CHLORIDE, DBASIC SODIUM PHOSPHATE, ESSENTIAL OIL BLEND (CONSISTING OF WINTERGREEN OIL, SPEARMINT OIL, PEPPERMINT OIL, AND EUCALYPTUS OIL), MONOBASIC SODIUM PHOSPHATE, POLYSORBATE 80, PROPYLENE GLYCOL, PURIFIED WATER, SODIUM CHLORIDE, AND SORBITOL SOLUTION SINOFRESH NASAL AND SINUS CARE eucalyptus globulus leaf, potassium dichromate liquid PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:59228-103 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF 20 [hp_X] in 100 mL POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 30 [hp_X] in 100 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) EMS Contract Packagi Llegiu el document complet