OCTISALATE,OCTOCRYLENE,OCTINOXATE,ZINC OXIDE,TITANIUM DIOXIDE,ENSULIZOLE

Product NDC
71801-542
11-digit product format
718010542
Labeler code
71801
Product ID
71801-542_bc8d9915-7e81-37e9-e053-2995a90a1cbf
Type
HUMAN OTC DRUG
Nonproprietary name
OCTISALATE,OCTOCRYLENE,OCTINOXATE,ZINC OXIDE,TITANIUM DIOXIDE,ENSULIZOLE
Dosage form
CREAM
Route
TOPICAL
Labeler
PROKPIL SAS
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-06-18
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE; OCTOCRYLENE; ENSULIZOLE; OCTINOXATE; OCTISALATE; ZINC OXIDE
Active strength
2 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71801-542-01OCTISALATE,OCTOCRYLENE,OCTINOXATE,ZINC OXIDE,TITANIUM DIOXIDE,ENSULIZOLE30 g in 1 BOXCREAM304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71801-542OCTISALATE,OCTOCRYLENE,OCTINOXATE,ZINC OXIDE,TITANIUM DIOXIDE,ENSULIZOLE CREAM [PROKPIL SAS]4Legacy NDC, 1 package rows20210303_6eafbc1c-44d8-5837-e053-2a91aa0ad979.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71801-542-017180105420130 g in 1 BOX (71801-542-01) 30 g2018-06-180000-00-00NoNoCurrent