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Product NDC
13537-683
11-digit product format
135370683
Labeler code
13537
Product ID
13537-683_7589969e-b476-421f-9d1c-77aaa50fd8dc
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate and Titanium Dioxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Ventura Corporation LTD
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2015-11-23
Marketing end
0000-00-00
Substance
OCTINOXATE; TITANIUM DIOXIDE
Active strength
0 g/mL; g/mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
13537-683-022025-03-20C16284748780-19d75b9d0-0727-f424-e053-dadaa90a57cee96fc142-e0e9-4f95-bd71-b3d7680a6df3
13537-683-022020-01-31C16284748780-19d75b9d0-0727-f424-e053-dadaa90a57cee96fc142-e0e9-4f95-bd71-b3d7680a6df3