Label: PHYTONCIDE SU- cypress distillate liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 75194-001-01, 75194-001-02, 75194-001-03 - Packager: Phytoncide Su Co LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated April 15, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
Put Phytoncide extract cypress water in a spray container and spray it all over the house.It captures unpleasant odors in the house, removes house dust mites, and has excellent antibacterial and deodorizing effects.It is made of natural materials, no harm to human body, relieve itching of the skin, improve rhinitis and asthma,If you smell the scent, you can reduce the stress hormone and you can feel the healing effect of forest bath in a recreational forest.To get a sleep effect, spray it before you sleep. Eliminates various oders from food, blankets and wardrobes..
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WARNINGS
Precautions
1. It is harmless to human body, but do not drink it
2. Avoid direct sunlight and store in a cool place
3. Keep it in a closed place in children's hands
4. Do not keep the lid open.
First Aid General
If medical action is required, show the product's container
or labeling information, and if you feel uncomfortable with
exposure to the product, a medical institution (please seek
help from a doctor)
Oral exposure: If it gets into your eyes, wash it away
immediately and consult your doctor if you have any
abnormalities.
Quality management and quality labeling under the
Industrial Products Safety Management Act - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PHYTONCIDE SU
cypress distillate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75194-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62) (CHAMAECYPARIS OBTUSA WOOD OIL - UNII:P2OMP71Y62) CHAMAECYPARIS OBTUSA WOOD OIL 10 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CHAMAECYPARIS OBTUSA WHOLE (UNII: 80ZNL1G5XY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75194-001-02 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2020 2 NDC:75194-001-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2020 3 NDC:75194-001-03 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/2020 Labeler - Phytoncide Su Co LTD (695625997) Registrant - Phytoncide Su Co LTD (695625997) Establishment Name Address ID/FEI Business Operations Phytoncide Su Co LTD 695625997 manufacture(75194-001)