Home NDC 80782-001-01 Day in the sun kit
Product NDC 80782-001
Requested package NDC 80782-001-01
11-digit product format 807820001
Labeler code 80782
Product ID 80782-001_cc350a9c-e1d6-4e9c-e053-2a95a90ab810
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE
Dosage form KIT
Labeler THE WONDERFUL GROUP LLC
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2021-08-01
Marketing end 0000-00-00
Active strength 0
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 · 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.
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 80782-001-01 Day in the sun kit 1 in 1 KIT KIT 1 2 80782-002-01 Day in the sun kit 75 mL in 1 TUBE LOTION 75 mL 8 g in 100mL 2 80782-003-01 Day in the sun kit 50 mL in 1 JAR CREAM 50 mL 9 g in 100mL 2 80782-004-01 Day in the sun kit 4.5 g in 1 TUBE GEL 4.5 g 5 g in 100g 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80782-001 DAY IN THE SUN KIT (AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE) KIT [THE WONDERFUL GROUP LLC] 2 Legacy NDC, 4 package rows 20230125_2c8ab6f2-930e-47e4-946a-965df238e05e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 80782-001-01 80782000101 1 KIT in 1 KIT (80782-001-01) * 75 mL in 1 BOTTLE * 75 mL in 1 TUBE (80782-002-01) * 50 mL in 1 JAR (80782-003-01) * 75 mL in 1 BOTTLE * 4.5 g in 1 TUBE (80782-004-01) 1 kit 2021-08-01 0000-00-00 No No Current