Home NDC 82931-004-19 Sand Sky Australian Sunshield Body Sunscreen SPF50 plus
Product NDC 82931-004
Requested package NDC 82931-004-19
11-digit product format 829310004
Labeler code 82931
Product ID 82931-004_16e5b75e-6282-4df4-8f63-4a60bea58b85
Type HUMAN OTC DRUG
Nonproprietary name Sand Sky Australian Sunshield Body Sunscreen spf50 plus
Dosage form LOTION
Route TOPICAL
Labeler Supernova USA Inc.
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2023-01-04
Marketing end 0000-00-00
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 3 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.
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 82931-004-19 Sand Sky Australian Sunshield Body Sunscreen SPF50 plus 1 in 1 CARTON LOTION 1 1 82931-004-19 Sand Sky Australian Sunshield Body Sunscreen SPF50 plus 190 mL in 1 BOTTLE, PLASTIC LOTION 190 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82931-004 SAND SKY AUSTRALIAN SUNSHIELD BODY SUNSCREEN SPF50 PLUS LOTION [SUPERNOVA USA INC.] 1 Legacy NDC, 2 package rows 20230105_1ed8e7d6-4fa4-4725-9aa5-5861027a537e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 82931-004-19 82931000419 1 BOTTLE, PLASTIC in 1 CARTON (82931-004-19) > 190 mL in 1 BOTTLE, PLASTIC 2023-01-04 0000-00-00 No No Current