HYDRO SPLASH BB

Product NDC
51523-012
11-digit product format
515230012
Labeler code
51523
Product ID
51523-012_2c75cdc9-d568-4d54-84d5-9447395ebd7f
Type
HUMAN OTC DRUG
Nonproprietary name
TITANIUM DIOXIDE
Dosage form
CREAM
Route
CUTANEOUS
Labeler
THEFACESHOP CO., LTD.
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2008-07-01
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE
Active strength
4 g/45g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51523-012-012019-10-21C16284748780-1956f9ecf-bd69-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-012-01HYDRO SPLASH BBSPF20 PA45 g in 1 CARTONCREAM451

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JPHYDRO SPLASH BB SPF20 PA (TITANIUM DIOXIDE) CREAM [THEFACESHOP CO., LTD.]1
TITANIUMACTIVE MOIETYD1JT611TNEHYDRO SPLASH BB SPF20 PA (TITANIUM DIOXIDE) CREAM [THEFACESHOP CO., LTD.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-012HYDRO SPLASH BB SPF20 PA (TITANIUM DIOXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 1 package rows20100714_03382d4f-0241-43c6-b6b6-b6c6ccd05b50.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
51523-012-015152300120145 g in 1 CARTON45 gHistorical