Label: MOSQUITOES GO AWAY- chamaecyparis obtusa oil liquid
- NDC Code(s): 84442-0001-1
- Packager: Poongkyung CNC Corp.
- 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 June 24, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
● 12 years of age or older~Adults: Apply an appropriate amount to exposed areas
such as the face (excluding eyes and mouth area), neck, arms, and legs. ● 2years of age or older
to under 12 years of age: Apply a small amount to exposed areas, excludingthe face and hands,
once to three times a day. ●6 months or more ~under 2 years old: Apply a small amount once a
day to exposed areas except the face and hands (but only used in situations where there is a very
high risk of infection due to insect bites). ● Less than 6 months: Do not use it.
① If there are any abnormal symptoms or side effects such as red spots,
swelling, or itching due to direct sunlight, consult with a specialist, etc. ② Do not use it on injured
areas.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MOSQUITOES GO AWAY
chamaecyparis obtusa oil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84442-0001 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 25.5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84442-0001-1 17 mL in 1 CONTAINER; Type 0: Not a Combination Product 06/25/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/25/2024 Labeler - Poongkyung CNC Corp. (687910361) Registrant - Poongkyung CNC Corp. (687910361) Establishment Name Address ID/FEI Business Operations Poongkyung CNC Corp. 687910361 manufacture(84442-0001)