Home NDC 0316-2075-50 Blue Lizard Sport SPF 50 Sunscreen
Product NDC 0316-2075
Requested package NDC 0316-2075-50
11-digit product format 003162075
Labeler code 0316
Product ID 0316-2075_ce55c08b-e83f-024b-e053-2995a90a6681
Type HUMAN OTC DRUG
Nonproprietary name Octisalate and Titanium Dioxide and Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Crown Laboratories
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2021-02-09
Marketing end 0000-00-00
Substance OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength 56 mg/mL; mg/mL; mg/mL
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0316-2075 0316-2075-50 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0316-2075 0316-2075-50 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Blue Lizard Sport SPF 50 Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 55.5 mg/mL TITANIUM DIOXIDE 59.5 mg/mL ZINC OXIDE 111 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup 15FIX9V2JP Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 0316-2075-30 Blue Lizard Sport SPF 50 Sunscreen 89 mL in 1 TUBE LOTION 89 8 0316-2075-40 Blue Lizard Sport SPF 50 Sunscreen 148 mL in 1 BOTTLE, PLASTIC LOTION 148 8 0316-2075-40 Blue Lizard Sport SPF 50 Sunscreen 1 in 1 CARTON LOTION 1 8 0316-2075-45 Blue Lizard Sport SPF 50 Sunscreen 148 mL in 1 TUBE LOTION 148 8 0316-2075-50 Blue Lizard Sport SPF 50 Sunscreen 259 mL in 1 BOTTLE, PLASTIC LOTION 259 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0316-2075 BLUE LIZARD SPORT SPF 50 SUNSCREEN (OCTISALATE AND TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [CROWN LABORATORIES] 4 Legacy NDC, 5 package rows 20231205_4955fa1c-789d-4f42-af75-70223310644a.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0316-2075-50 00316207550 259 mL in 1 BOTTLE, PLASTIC (0316-2075-50) 259 ml 2021-05-01 0000-00-00 No No Current