Home NDC 81120-109-01 Celesty
Product NDC 81120-109
Requested package NDC 81120-109-01
11-digit product format 811200109
Labeler code 81120
Product ID 81120-109_d5d692e5-6286-4a01-963e-dd89097b773e
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Avobenzone, Octocrylene, Octinoxate
Dosage form CREAM
Route TOPICAL
Labeler MABA KOZMETIK LIMITED SIRKETI
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-12-07
Marketing end 0000-00-00
Substance HOMOSALATE; AVOBENZONE; OCTOCRYLENE; OCTINOXATE
Active strength 64 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 · 16 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 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…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…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…
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 81120-109-01 CelestySun Protection Series Solar Protection Fluid SPF 50 75 mL in 1 TUBE CREAM 75 1 81120-109-01 CelestySun Protection Series Solar Protection Fluid SPF 50 1 in 1 BOX CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81120-109 CELESTY SUN PROTECTION SERIES SOLAR PROTECTION FLUID SPF 50 (HOMOSALATE, AVOBENZONE, OCTOCRYLENE, OCTINOXATE) CREAM [MABA KOZMETIK LIMITED SIRKETI] 1 Legacy NDC, 2 package rows 20210109_7bd1a7ed-139d-4c30-9e86-010b7eb85c19.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81120-109-01 81120010901 1 TUBE in 1 BOX (81120-109-01) > 75 mL in 1 TUBE 1 tube 2020-12-07 0000-00-00 No No Current