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

Antiseptic

Uses

First aid to help protect against bacterial contamination.

WARNINGS

For external use only.

Do not use in the eyes or apply over large areas of the body.

In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.

Stop use and ask a doctor if the condition persists or gets worse.

Do not use longer than 1 week unless directed by a doctor.

For external use only.

Do not use on wounds or damaged skin, with a heating pad or on a child under 12 years of age

FLAMMABLE:

Keep away from fire or flame.

ASK A DOCTOR BEFORE USE IF

If you have redness over affected area.

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

Clean the affected area.

Spray two to three pumps or as necessary to cover the affected area 1 or 3 times daily.

May be covered with a sterile bandage.

If bandaged, let dry first. Children under 12 years of age: do not use, consult a doctor.

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 - ANTISEPTIC PEDI SPRAY 4 oz

FOOTSPA - ANTISEPTIC PEDI SPRAY 16 oz

FOOTSPA - ANTISEPTIC PEDI SPRAY 128 oz

INGREDIENTS AND APPEARANCE

FOOTSPA PEDI 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49283-702
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: 49283-702-16	473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/30/2025
2	NDC: 49283-702-04	118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/30/2025
3	NDC: 49283-702-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/30/2025

Labeler - CHEMCO CORPORATION (032495954)