Home NDC 76731-204-01 CELGEN MILD SUN
Product NDC 76731-204
Requested package NDC 76731-204-01
11-digit product format 767310204
Labeler code 76731
Product ID 76731-204_ae604fe2-8252-555e-e053-2995a90ac018
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, OCTISALATE, BEMOTRIZINOL, TITANIUM DIOXIDE, ETHYLHEXYL TRIAZONE, AVOBENZONE
Dosage form CREAM
Route TOPICAL
Labeler BBHC CO., LTD
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-09-03
Marketing end 0000-00-00
Substance TITANIUM DIOXIDE; ETHYLHEXYL TRIAZONE; AVOBENZONE; OCTINOXATE; OCTISALATE; BEMOTRIZINOL
Active strength 2 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g
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 · 18 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…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
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 76731-204-01 CELGEN MILD SUN 50 g in 1 TUBE CREAM 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76731-204 CELGEN MILD SUN (OCTINOXATE, OCTISALATE, BEMOTRIZINOL, TITANIUM DIOXIDE, ETHYLHEXYL TRIAZONE, AVOBENZONE) CREAM [BBHC CO., LTD] 1 Legacy NDC, 1 package rows 20200903_ae604fe2-8251-555e-e053-2995a90ac018.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76731-204-01 76731020401 50 g in 1 TUBE (76731-204-01) 50 g 2020-09-03 0000-00-00 No No Current