LOVLUV Vivacity Bright Cushion 21g

Product NDC
71909-0735
11-digit product format
719090735
Labeler code
71909
Product ID
71909-0735_b29d9a9d-5f40-b4e8-e053-2a95a90a0966
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, OCTINOXATE, ZINC OXIDE, OCTISALATE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Cnt Dream. Co., Ltd
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-01-31
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE; ZINC OXIDE; OCTINOXATE; OCTISALATE
Active strength
1 g/21g; g/21g; g/21g; g/21g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2022-08-30 03:57 UTC · source 2022-08-29excluded productproduct71909-0735IInactivated by FDAexcluded / ndc_excluded.zipfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproduct71909-0735IInactivated by FDAexcluded / ndc_excluded.zip86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproduct71909-0735IInactivated by FDAexcluded / ndc_excluded.zipbd6a592717d7…303034d00443…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#