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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

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct43596-0857DDiscontinued by firm2026-07-31
excluded packagepackage43596-085743596-0857-1DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

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