Home NDC 83071-060-02 Dr.Jucre Rebirth White Sun Protection
Product NDC 83071-060
Requested package NDC 83071-060-02
11-digit product format 830710060
Labeler code 83071
Product ID 83071-060_f667986b-9023-46e3-9f1f-6abb3162b5a1
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, HOMOSALATE, OCTISALATE, AVOBENZONE, ENSULIZOLE, OCTOCRYLENE, BEMOTRIZINOL, NIACINAMIDE, ADENOSINE
Dosage form CREAM
Route TOPICAL
Labeler NATURECELL CO., LTD.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-10-01
Marketing end 0000-00-00
Substance ADENOSINE; AVOBENZONE; BEMOTRIZINOL; ENSULIZOLE; HOMOSALATE; NIACINAMIDE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Active strength 0 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
Pharmacologic classes Adenosine Receptor Agonist [EPC], Adenosine Receptor Agonists [MoA]
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83071-060-01 Dr.Jucre Rebirth White Sun Protection 65 mL in 1 CONTAINER CREAM 65 1 83071-060-02 Dr.Jucre Rebirth White Sun Protection 1 in 1 CARTON CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83071-060 DR.JUCRE REBIRTH WHITE SUN PROTECTION (OCTINOXATE, HOMOSALATE, OCTISALATE, AVOBENZONE, ENSULIZOLE, OCTOCRYLENE, BEMOTRIZINOL, NIACINAMIDE, ADENOSINE) CREAM [NATURECELL CO., LTD.] 1 Legacy NDC, 2 package rows 20221109_2bdb15b8-59d4-4523-bafb-82b81f2771d9.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 83071-060-02 83071006002 1 CONTAINER in 1 CARTON (83071-060-02) > 65 mL in 1 CONTAINER (83071-060-01) 1 container 2022-10-01 0000-00-00 No No Current