Double Use Compact SPF 15 gold deluxe edition Medium 7

Product NDC
43596-0193
11-digit product format
435960193
Labeler code
43596
Product ID
43596-0193_b5e8b186-477a-0b22-e053-2995a90a4c76
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Titanium dioxide, Zinc Oxide
Dosage form
POWDER
Route
TOPICAL
Labeler
Ventura Corporation LTD
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2020-11-12
Marketing end
0000-00-00
Substance
ZINC OXIDE; TITANIUM DIOXIDE; OCTINOXATE
Active strength
5 g/100g; g/100g; 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 productproduct43596-0193DDiscontinued by firm2026-07-31
excluded packagepackage43596-019343596-0193-1DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43596-0193-14359601930110 g in 1 BOTTLE (43596-0193-1) 10 g2020-11-120000-00-00NoNoCurrent