Esika Pro Compact High Definintion and Double Finish SPF 15

Product NDC
43596-0059
11-digit product format
435960059
Labeler code
43596
Product ID
43596-0059_ab40e923-55be-442d-bbdf-2a4d16c91e63
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Titanium Dioxide, and Zinc Oxide
Dosage form
POWDER
Route
TOPICAL
Labeler
Ventura Corporation LTD
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-04-16
Marketing end
0000-00-00
Substance
OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
0 g/g; g/g; g/g
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
43596-0059-22025-04-06C16284748780-19d75b9d0-da14-f424-e053-dadaa90a57ce7cc0a280-b108-47ec-9aa2-a111253006d3
43596-0059-22020-01-31C16284748780-19d75b9d0-da14-f424-e053-dadaa90a57ce7cc0a280-b108-47ec-9aa2-a111253006d3