OCTINOXATE,OCTISALATE,AVOBENZONE,OCTOCRYLENE,ENSULIZOLE,TITANIUM DIOXIDE

Product NDC
71801-541
11-digit product format
718010541
Labeler code
71801
Product ID
71801-541_ba61353d-f750-704e-e053-2995a90abbf2
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE,OCTISALATE,AVOBENZONE,OCTOCRYLENE,ENSULIZOLE,TITANIUM DIOXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
PROKPIL SAS
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-09-01
Marketing end
0000-00-00
Substance
OCTISALATE; OCTOCRYLENE; ENSULIZOLE; AVOBENZONE; OCTINOXATE; TITANIUM DIOXIDE
Active strength
5 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
71801-541-01OCTINOXATE,OCTISALATE,AVOBENZONE,OCTOCRYLENE,ENSULIZOLE,TITANIUM DIOXIDE30 g in 1 BOXCREAM305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71801-541OCTINOXATE,OCTISALATE,AVOBENZONE,OCTOCRYLENE,ENSULIZOLE,TITANIUM DIOXIDE CREAM [PROKPIL SAS]5Legacy NDC, 1 package rows20210303_5c4230af-280e-2b73-e053-2991aa0aa4a9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71801-541-017180105410130 g in 1 BOX (71801-541-01) 30 g2017-09-010000-00-00NoNoCurrent