RECIPE Infinite UV Shield Sunscreen Broad Spectrum SPF100

Product NDC
80670-001
11-digit product format
806700001
Labeler code
80670
Product ID
80670-001_d1f06b5a-744e-cbde-e053-2a95a90a5ea9
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
BAY BELLE LABS
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-09-17
Marketing end
0000-00-00
Substance
HOMOSALATE; AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OCTISALATE
Active strength
90 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2022-12-31
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 · 10 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage80670-001-00367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage80670-001-00557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28excluded productproduct8af77b9d5b6f…d9bbb34c5368…
2024-05-28 21:12 UTC · source 2024-05-28excluded packagepackage80670-001-008af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14excluded productproduct834df4deac94…adcc014656a3…
2024-05-15 03:39 UTC · source 2024-05-14excluded packagepackage80670-001-00834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08excluded productproduct1332a3947898…d4bfe170f9cd…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage80670-001-001332a3947898…d4bfe170f9cd…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80670-001-002023-01-30C16284748780-1f386c649-fa79-0266-e053-dadaa90a7c1ab0254b0c-325f-96d9-e053-2a95a90ad8b4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
80670-001-00806700001001 BOTTLE in 1 CARTON (80670-001-00) > 50 mL in 1 BOTTLE1 bottle2020-09-170000-00-00NoNoCurrent