FOOTSPA PEDI- alcohol spray 
CHEMCO CORPORATION

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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49283-707-16
49283-707-04
49283-707-01

Ethyl Alcohol 70%v/v

Antimicrobial

USES:

To decrease bacteria on the skin.

• For external use only.

• Avoid contact with eyes or mucous membrane.

• Do not apply to wounds or damaged
skin with a heating pad or on a child
under 12 year of age.

FLAMMABLE:

Keep away from fire or flame.

ASK A DOCTOR BEFORE USE IF

If you have redness over affected area.

Condition persists for more than 72 hours.

If swallowed, get medical help, or contact a Poison Control Center right away.

DIRECTIONS:

Adults and children 12 years of age or older
• Spray two to three pumps or as
necessary to cover the affected area
not more than three to four times
daily.

Water (Aqua), Camphor, Polysorbate 20, Menthol, DMDM Hydantoin, Mentha Piperita (Peppermint) Oil, Eucalyptus Globulus Leaf Oil, D&C Yellow No.11(CI 47000), FD&C Blue No.1 (CI 42090).

Contact us
+1 (305) 623-4445

FOOTSPA - ANTIBACTERIAL PEDI SPRAY 4 oz

PEDI SPRAY 4

FOOTSPA - ANTIBACTERIAL PEDI SPRAY 16 oz

PEDI SPRAY 16

FOOTSPA - ANTIBACTERIAL PEDI SPRAY 128 oz

PEDI SPRAY 1

FOOTSPA PEDI 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49283-707
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
MENTHOL (UNII: L7T10EIP3A)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
D&C YELLOW NO. 11 (UNII: 44F3HYL954)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
Product Characteristics
ColorgreenScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49283-707-16473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/08/2023
2NDC:49283-707-04118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/08/2023
3NDC:49283-707-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product09/08/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/17/2021
Labeler - CHEMCO CORPORATION (032495954)
Registrant - CHEMCO CORPORATION (032495954)
Establishment
NameAddressID/FEIBusiness Operations
CHEMCO CORPORATION032495954manufacture(49283-707)

Revised: 9/2023
Document Id: 04de86a2-835e-cbce-e063-6294a90a4956
Set id: 04de4392-74f6-7df8-e063-6294a90ae3b1
Version: 1
Effective Time: 20230908
 
CHEMCO CORPORATION