Home NDC 76144-915-01 Paulas Choice Resist Smoothing Primer Serum SPF 30
Product NDC 76144-915
Requested package NDC 76144-915-01
11-digit product format 761440915
Labeler code 76144
Product ID 76144-915_c54ddd72-5d5d-218c-e053-2995a90a7cee
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octinoxate, Octisalate
Dosage form GEL
Route TOPICAL
Labeler Paula's Choice, LLC
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-02-01
Marketing end 0000-00-00
Substance AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE
Active strength 2 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2023-12-31
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 76144-915 76144-915-01 I Inactivated by FDA excluded / ndc_excluded.zip e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 76144-915 76144-915-01 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 76144-915-01 76144091501 1 TUBE in 1 CARTON (76144-915-01) > 30 mL in 1 TUBE (76144-915-00) 1 tube 2017-02-01 0000-00-00 No No Current