Rejuvaderm Medispa sunscreen

Product NDC
51325-100
11-digit product format
513250100
Labeler code
51325
Product ID
51325-100_2cd3a7e4-1a01-465c-a413-609709103087
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Octisalate, Zinc oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Ellen H Frankle MD Inc
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-08-01
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTISALATE; ZINC OXIDE
Active strength
9 mL/120mL; mL/120mL; mL/120mL
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
51325-100-012019-10-21C16284748780-1956f9ecf-cadd-621f-e053-dbdaa90a74adRejuvaderm Medispa Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51325-100-01Rejuvaderm Medispa sunscreen120 mL in 1 TUBELOTION1201

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51325-100REJUVADERM MEDISPA SUNSCREEN (OCTINOXATE, OCTISALATE, ZINC OXIDE) LOTION [ELLEN H FRANKLE MD INC]1Legacy NDC, 1 package rows20100825_1cf73889-aa5f-4a87-8584-348d6192dc24.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
51325-100-0151325010001120 mL in 1 TUBE120 mlHistorical