FOOTSPA PEDI- alcohol spray

FOOTSPA PEDI by

Drug Labeling and Warnings

FOOTSPA PEDI by is a Otc medication manufactured, distributed, or labeled by CHEMCO CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 70%v/v

PURPOSE

Antimicrobial

USES:

To decrease bacteria on the skin.

WARNINGS

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.

STOP USE

Condition persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

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.

INACTIVE INGREDIENT

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).

QUESTIONS

Contact us
+1 (305) 623-4445

FOOTSPA - ANTIBACTERIAL PEDI SPRAY 4 oz

FOOTSPA - ANTIBACTERIAL PEDI SPRAY 16 oz

FOOTSPA - ANTIBACTERIAL PEDI SPRAY 128 oz

INGREDIENTS AND APPEARANCE

FOOTSPA PEDI 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49283-707
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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
Color	green	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49283-707-16	473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/08/2023
2	NDC: 49283-707-04	118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/08/2023
3	NDC: 49283-707-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/08/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/17/2021

Labeler - CHEMCO CORPORATION (032495954)

Registrant - CHEMCO CORPORATION (032495954)

Establishment
Name	Address	ID/FEI	Business Operations
CHEMCO CORPORATION		032495954	manufacture(49283-707)