Double Use Compact SPF 15 gold deluxe edition Medium 7

Product NDC
14783-279
11-digit product format
147830279
Labeler code
14783
Product ID
14783-279_b5f80d1f-f8cd-70b4-e053-2995a90a86ee
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Titanium dioxide, Zinc Oxide
Dosage form
POWDER
Route
TOPICAL
Labeler
Ventura International 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 productproduct14783-279DDiscontinued by firm2026-07-31
excluded packagepackage14783-27914783-279-01DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
14783-279-011478302790110 g in 1 BOTTLE (14783-279-01) 10 g2020-11-120000-00-00NoNoCurrent