PENGSPRAY- cypress oil, eucalyptus oil, coral calcium spray 
CA GLOBAL

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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83635-301 PENG SPRAY

Active Ingredients

Cypress oil, Eucalyptus oil, Coral calcium (CT-CCP50)

Purposes

Cypress oil0.5%w/w................................................... Disinfection

Eucalyptus oil 0.1% w/w............................................. Disinfection

Coral calcium (CT-CCP50) 0.0053% w/w .................. Disinfection

Uses

Disinfection and odor elimination of indoor spaces and objects.

Warnings

Do not use for the purpose other than described above.

Warnings

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right way.

Warnings

Stop use and ask a doctor r appears any allergic symptom.

Warnings

When using this product keep out of eyes, ears, and mouth.

Warnings

For external use only.

Directions

Shake the product well and spray at 30~40 cm distance from the place where needs disinfection or elimination of odor.

Inactive Ingredients

polysorbate 80, water

Label

Peng Spray Label

PENGSPRAY 
cypress oil, eucalyptus oil, coral calcium spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83635-301
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL0.1 g  in 100 mL
CUPRESSUS SEMPERVIRENS LEAF OIL (UNII: M7QUY89S4O) (CUPRESSUS SEMPERVIRENS LEAF OIL - UNII:M7QUY89S4O) CUPRESSUS SEMPERVIRENS LEAF OIL0.5 g  in 100 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE0.0053 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83635-301-01300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/16/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/16/2023
Labeler - CA GLOBAL (690049071)
Registrant - CA GLOBAL (690049071)
Establishment
NameAddressID/FEIBusiness Operations
CA GLOBAL690049071manufacture(83635-301)

Revised: 7/2023
Document Id: 0137f663-fccf-9d31-e063-6394a90a4897
Set id: 0137f663-fcce-9d31-e063-6394a90a4897
Version: 1
Effective Time: 20230724
 
CA GLOBAL