Home NDC 69039-212-03 SUN BUM SPF 15 PREMIUM MOISTURIZING SUNSCREEN
Product NDC 69039-212
Requested package NDC 69039-212-03
11-digit product format 690390212
Labeler code 69039
Product ID 69039-212_d912dabd-2535-7b4e-e053-2995a90ae323
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form LOTION
Route TOPICAL
Labeler Sun Bum, LLC.
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2022-02-16
Marketing end 0000-00-00
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 20 mg/mL; mg/mL; mg/mL; mg/mL
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 69039-212-01 Sun Bum SPF 15 Premium Moisturizing Sunscreen 1 in 1 BOX LOTION 1 4 69039-212-01 Sun Bum SPF 15 Premium Moisturizing Sunscreen 237 mL in 1 BOTTLE LOTION 237 4 69039-212-03 SUN BUM SPF 15 PREMIUM MOISTURIZING SUNSCREEN 3780 mL in 1 BOTTLE LOTION 3780 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69039-212 SUN BUM SPF 15 PREMIUM MOISTURIZING SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [SUN BUM, LLC] 4 Legacy NDC, 2 package rows 20220205_ead6d23a-b0ad-4cc9-a1cb-666b0bcd8b3a.zip 69039-212 SUN BUM SPF 15 PREMIUM MOISTURIZING SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [SUN BUM, LLC.] 1 Legacy NDC, 1 package rows 20220301_d912d9ba-0203-05f6-e053-2995a90a58d1.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69039-212-03 69039021203 3780 mL in 1 BOTTLE (69039-212-03) 3780 ml 2022-02-16 0000-00-00 No No Current