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Product NDC
13537-714
11-digit product format
135370714
Labeler code
13537
Product ID
13537-714_7d329a3b-e8e8-47eb-bfdb-56f179407526
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate
Dosage form
LIPSTICK
Route
TOPICAL
Labeler
Ventura Corporation LTD
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2015-12-14
Marketing end
0000-00-00
Substance
OCTINOXATE
Active strength
0 g/g
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
13537-714-022025-03-24C16284748780-19d75b9d0-fbd7-f424-e053-dadaa90a57ce923a39ce-7793-4596-ad1a-52ffe9e396de
13537-714-022020-01-31C16284748780-19d75b9d0-fbd7-f424-e053-dadaa90a57ce923a39ce-7793-4596-ad1a-52ffe9e396de