Brillie Ultimate Soothing Sun Shield

Product NDC
80134-050
11-digit product format
801340050
Labeler code
80134
Product ID
80134-050_ad620c86-60dc-4428-e053-2a95a90aeb26
Type
HUMAN OTC DRUG
Nonproprietary name
Ethylhexyl Methoxycinnamate, Benzophenone-4, Titanium Dioxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Inhanzglobal Co.,Ltd
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-08-24
Marketing end
0000-00-00
Substance
OCTINOXATE; SULISOBENZONE
Active strength
3 g/50mL; g/50mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80134-050-022022-01-28C16284748780-1d6a99b39-c833-a426-e053-dadaa90af4c2Brillié Ultimate Soothing Sun Shield

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80134-050-01Brillie Ultimate Soothing Sun Shield50 mL in 1 TUBECREAM501
80134-050-02Brillie Ultimate Soothing Sun Shield1 in 1 BOXCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80134-050BRILLIE ULTIMATE SOOTHING SUN SHIELD (ETHYLHEXYL METHOXYCINNAMATE, BENZOPHENONE-4, TITANIUM DIOXIDE) CREAM [INHANZGLOBAL CO.,LTD]1Legacy NDC, 2 package rows20200824_ad620c86-60db-4428-e053-2a95a90aeb26.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
80134-050-018013400500150 mL in 1 TUBE50 mlHistorical
80134-050-02801340050021 TUBE in 1 BOX (80134-050-02) > 50 mL in 1 TUBE (80134-050-01) 1 tube2020-08-240000-00-00NoNoCurrent