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Product NDC
43596-0857
11-digit product format
435960857
Labeler code
43596
Product ID
43596-0857_b57fe0ef-0ca0-0c47-e053-2995a90a8faa
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate
Dosage form
POWDER
Route
TOPICAL
Labeler
Ventura Corporation LTD
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2020-04-01
Marketing end
0000-00-00
Substance
OCTINOXATE
Active strength
5 g/100g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43596-0857-12025-04-22C16284748780-1d6a99b3a-005d-a426-e053-dadaa90af4c2a2f2f918-fdb6-27c0-e053-2a95a90a4fb9
43596-0857-12022-01-28C16284748780-1d6a99b3a-005d-a426-e053-dadaa90af4c2a2f2f918-fdb6-27c0-e053-2a95a90a4fb9

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43596-0857-1435960857017 g in 1 CARTON (43596-0857-1) 7 g2020-04-010000-00-00NoNoCurrent