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Product NDC
13537-587
11-digit product format
135370587
Labeler code
13537
Product ID
13537-587_43e6be26-2591-47f9-92d5-3dccf3a32ed8
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
2015-04-17
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
13537-587-222025-02-28C16284748780-19d75b9d0-a5f4-f424-e053-dadaa90a57cef92b49ec-af7b-440f-a69b-d71b9f6dd5bf
13537-587-222020-01-31C16284748780-19d75b9d0-a5f4-f424-e053-dadaa90a57cef92b49ec-af7b-440f-a69b-d71b9f6dd5bf