FDA.reportPublic FDA data

FOOTSPA PEDI

Manufacturer
CHEMCO CORPORATION
Effective date
2025-11-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:43:00

Label at a glance#

ProductFOOTSPA PEDI
Active ingredientALCOHOL
Label structure14 sections

Indications and uses

To decrease bacteria on the skin.

Dosage and administration

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.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%v/v

OTC - PURPOSE SECTION

Antimicrobial

USES:

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

WARNINGS SECTION

• 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:

OTHER SAFETY INFORMATION

Keep away from fire or flame.

ASK A DOCTOR BEFORE USE IF

OTC - ASK DOCTOR SECTION

If you have redness over affected area.

OTC - STOP USE SECTION

Condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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 SECTION

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).

OTC - QUESTIONS SECTION

Contact us
+1 (305) 623-4445

FOOTSPA - ANTIBACTERIAL PEDI SPRAY 4 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PEDI SPRAY 4PEDI SPRAY 4

FOOTSPA - ANTIBACTERIAL PEDI SPRAY 16 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PEDI SPRAY 16PEDI SPRAY 16

FOOTSPA - ANTIBACTERIAL PEDI SPRAY 128 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PEDI SPRAY 1PEDI SPRAY 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN2
1041849ethanol 0.7 ML/ML Topical SpraySCD2
1041849ethanol 70 % Topical SpraySY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130755439025208GTIN-13: 0755439025208
EAN-13: 0755439025208
GTIN-12: 755439025208
UPC-A: 755439025208
GTIN storage (14 digits): 00755439025208		FD-00044 PEDI SPRAY 128 oz 49283-707-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49283-707-012025-11-08C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-012025-11-08C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-042025-11-08C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-042025-11-08C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-162025-11-08C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-162025-11-08C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-012025-01-30C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-012025-01-30C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-042025-01-30C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-042025-01-30C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-162025-01-30C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01
49283-707-162025-01-30C16284748780-12cef2736-a62c-d83d-e063-dadaa90ab31f49283-707-16 49283-707-04 49283-707-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49283-707-01FOOTSPA PEDI3785 mL in 1 BOTTLESPRAY37852
49283-707-04FOOTSPA PEDI118 mL in 1 BOTTLE, SPRAYSPRAY1182
49283-707-16FOOTSPA PEDI473 mL in 1 BOTTLE, SPRAYSPRAY4732

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49283-70749283-707-16, 49283-707-04, 49283-707-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLYSORBATE 207T1F30V5YHIACT
MENTHOLL7T10EIP3AIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
ALCOHOL3K9958V90MACTIB
PEPPERMINT OILAV092KU4JHIACT
EUCALYPTUS OIL2R04ONI662IACT
D&C YELLOW NO. 1144F3HYL954IACT
DMDM HYDANTOINBYR0546TOWIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12023-09-08full-release2026-05-31 23:56:10

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FOOTSPA PEDIALCOHOLCHEMCO CORPORATION04de4392-74f6-7df8-e063-6294a90ae3b12025-11-08WarningsExact identifier
ndc (package): 49283-707-04
ndc (package): 49283-707-16
ndc (package): 49283-707-01
ndc (product): 49283-707
ndc11 (package): 49283070716
ndc11 (package): 49283070704
ndc11 (package): 49283070701
spl id: 4318c0bb-2dca-29a7-e063-6394a90ac2ea
spl set id: 04de4392-74f6-7df8-e063-6294a90ae3b1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.