Medi UV Block Suncream SPF50 PA

Product NDC
43948-8001
11-digit product format
439488001
Labeler code
43948
Product ID
43948-8001_946e823a-ff0c-4976-9a94-0b0675f49543
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE OCTOCRYLENE
Dosage form
CREAM
Route
TOPICAL
Labeler
The Doctor's Cosmetic Inc
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2009-11-01
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTOCRYLENE
Active strength
3 mL/60mL; mL/60mL
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
43948-8001-12019-10-21C16284748780-1956f9ecf-c4dd-621f-e053-dbdaa90a74ad473d1c05-b10b-4480-86bd-4541c042f508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43948-8001-1Medi UV Block Suncream SPF50 PA60 mL in 1 TUBECREAM602

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43948-8001MEDI UV BLOCK SUNCREAM SPF50 PA (OCTINOXATE OCTOCRYLENE) CREAM [THE DOCTOR'S COSMETIC INC]2Legacy NDC, 1 package rows20091208_473d1c05-b10b-4480-86bd-4541c042f508.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
43948-8001-14394880010160 mL in 1 TUBE60 mlHistorical