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.

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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:

ASK A DOCTOR BEFORE USE IF YOU HAVE

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

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

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SINOFRESH  NASAL AND SINUS CARE
eucalyptus globulus leaf, potassium dichromate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59228-103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF20 [hp_X]  in 100 mL
POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE30 [hp_X]  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
SPEARMINT OIL (UNII: C3M81465G5)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SORBITOL (UNII: 506T60A25R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59228-103-1129.6 mL in 1 BOTTLE; Type 0: Not a Combination Product05/30/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/30/2014
Labeler - EMS Contract Packaging (048602791)

Revised: 4/2022
Document Id: dd463d5c-cb68-c72f-e053-2a95a90a0ecc
Set id: e1cdfbed-54d9-452b-bf0c-d62c1b9b2c9e
Version: 9
Effective Time: 20220422
 
EMS Contract Packaging