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Product NDC
43596-0208
11-digit product format
435960208
Labeler code
43596
Product ID
43596-0208_c07f9ec6-7302-2f48-e053-2a95a90a56ea
Type
HUMAN OTC DRUG
Nonproprietary name
zinc oxide,octinoxate
Dosage form
EMULSION
Route
TOPICAL
Labeler
Ventura Corporation LTD
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-04-14
Marketing end
0000-00-00
Substance
OCTINOXATE; ZINC OXIDE
Active strength
5 g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43596-0208-12025-04-22C16284748780-1f386c649-b14f-0266-e053-dadaa90a7c1ac07f9ec6-7301-2f48-e053-2a95a90a56ea
43596-0208-12023-01-30C16284748780-1f386c649-b14f-0266-e053-dadaa90a7c1ac07f9ec6-7301-2f48-e053-2a95a90a56ea

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43596-0208-14359602080130 mL in 1 JAR (43596-0208-1) 30 ml2021-04-140000-00-00NoNoCurrent