Home NDC 80670-001-00 RECIPE Infinite UV Shield Sunscreen Broad Spectrum SPF100
Product NDC 80670-001
Requested package NDC 80670-001-00
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 · 5 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 80670-001-00 80670000100 1 BOTTLE in 1 CARTON (80670-001-00) > 50 mL in 1 BOTTLE 1 bottle 2020-09-17 0000-00-00 No No Current