FDA.reportPublic FDA data

FOOTSPA PEDI

Product NDC
49283-702
11-digit product format
492830702
Labeler code
49283
Product ID
49283-702_4c25a816-65f9-6189-e063-6294a90a4d04
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
SPRAY
Route
TOPICAL
Labeler
CHEMCO CORPORATION
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-06-30
Substance
ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
FOOTSPA PEDI
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL70 mL/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M
Rxcui1041849

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49283-702-01FOOTSPA PEDI3785 mL in 1 BOTTLESPRAY37852
49283-702-04FOOTSPA PEDI118 mL in 1 BOTTLE, SPRAYSPRAY1182
49283-702-16FOOTSPA PEDI473 mL in 1 BOTTLE, SPRAYSPRAY4732

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1041849ethanol 70 % Topical SprayPSN3886a958-d035-ed15-e063-6294a90af1b52
1041849ethanol 0.7 ML/ML Topical SpraySCD3886a958-d035-ed15-e063-6294a90af1b52
1041849ethanol 70 % Topical SpraySY3886a958-d035-ed15-e063-6294a90af1b52

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
49283-702-01492830702013785 mL in 1 BOTTLE (49283-702-01) 3785 ml2025-06-30NoNoHistorical
49283-702-0449283070204118 mL in 1 BOTTLE, SPRAY (49283-702-04) 118 ml2025-06-30NoNoHistorical
49283-702-1649283070216473 mL in 1 BOTTLE, SPRAY (49283-702-16) 473 ml2025-06-30NoNoHistorical