Home NDC 46007-201-25 AGE DEFYING HYDRATING SUNSCREEN
Product NDC 46007-201
Requested package NDC 46007-201-25
11-digit product format 460070201
Labeler code 46007
Product ID 46007-201_d53e0ec1-2b76-48c5-e053-2a95a90aba3e
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE
Dosage form LOTION
Route TOPICAL
Labeler Skin Authority LLC
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2012-04-19
Marketing end 0000-00-00
Substance AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE; HOMOSALATE; OCTOCRYLENE
Active strength 3 g/100mL; g/100mL; 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 · 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 46007-201-25 AGE DEFYING HYDRATING SUNSCREENSPF 30 150 mL in 1 TUBE LOTION 150 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 46007-201 AGE DEFYING HYDRATING SUNSCREEN SPF 30 (AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE) LOTION [SKIN AUTHORITY LLC] 6 Legacy NDC, 1 package rows 20231208_54634312-6831-4c42-badc-cdd77438a6b0.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 46007-201-25 46007020125 150 mL in 1 TUBE (46007-201-25) 150 ml 2012-04-19 0000-00-00 No No Current