Home NDC 73655-090-02 CELONIA SIGNATURE BIO TONE UP SUN BLOCK
Product NDC 73655-090
Requested package NDC 73655-090-02
11-digit product format 736550090
Labeler code 73655
Product ID 73655-090_3bcd8375-6e4c-440a-aad4-c002fce3740b
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, Titanium Dioxide, Avobenzone
Dosage form CREAM
Route TOPICAL
Labeler Celino Inc.
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-02-01
Marketing end 0000-00-00
Substance HOMOSALATE; OCTISALATE; TITANIUM DIOXIDE; AVOBENZONE
Active strength 5 g/50mL; g/50mL; g/50mL; g/50mL
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 · 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73655-090-01 CELONIA SIGNATURE BIO TONE UP SUN BLOCK 50 mL in 1 CONTAINER CREAM 50 1 73655-090-02 CELONIA SIGNATURE BIO TONE UP SUN BLOCK 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 73655-090 CELONIA SIGNATURE BIO TONE UP SUN BLOCK (HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, AVOBENZONE) CREAM [CELINO INC.] 1 Legacy NDC, 2 package rows 20200310_24fe5112-e318-4d46-ad33-b3dc53ec07f6.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 73655-090-02 73655009002 1 CONTAINER in 1 CARTON (73655-090-02) > 50 mL in 1 CONTAINER (73655-090-01) 1 container 2020-02-01 0000-00-00 No No Current