Cicatricure Brightening Face With SPF

Product NDC
50066-704
11-digit product format
500660704
Labeler code
50066
Product ID
50066-704_c60e33d1-3c88-4fcb-8af4-f13332961632
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octinoxate, Octisalate, and Oxybenzone
Dosage form
CREAM
Route
TOPICAL
Labeler
Genomma Lab USA
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-10-07
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength
10 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct50066-704DDiscontinued by firm2026-10-20
excluded packagepackage50066-70450066-704-01DDiscontinued by firm2026-10-20

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50066-704CICATRICURE BRIGHTENING WITH SPF SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, AND OXYBENZONE) CREAM [GENOMMA LAB USA]5Legacy NDC20241206_3509540e-636f-4eb9-91e6-8c37dbbc16ba.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50066-704-01500660704011 BOTTLE, PLASTIC in 1 CARTON (50066-704-01) > 50 mL in 1 BOTTLE, PLASTIC2019-10-070000-00-00NoNoCurrent