Blue Lizard Active SPF 50 Sunscreen

Product NDC: 0316-2072
Requested package NDC: 0316-2072-45
11-digit product format: 003162072
Labeler code: 0316
Product ID: 0316-2072_ce5337d4-bcfe-3886-e053-2a95a90af947
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	0316-2072	0316-2072-45	D	Discontinued by firm		2026-10-05

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, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
0316-2072-30	2023-02-13	Blue Lizard Active SPF 50 Sunscreen
0316-2072-40	2023-02-13	Blue Lizard Active SPF 50 Sunscreen
0316-2072-45	2023-02-13	Blue Lizard Active SPF 50 Sunscreen
0316-2072-50	2023-02-13	Blue Lizard Active SPF 50 Sunscreen
0316-2072-30	2023-01-30	Blue Lizard Active SPF 50 Sunscreen
0316-2072-40	2023-01-30	Blue Lizard Active SPF 50 Sunscreen
0316-2072-45	2023-01-30	Blue Lizard Active SPF 50 Sunscreen
0316-2072-50	2023-01-30	Blue Lizard Active SPF 50 Sunscreen

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0316-2072	BLUE LIZARD ACTIVE SPF 50 SUNSCREEN (OCTISALATE AND TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [CROWN LABORATORIES]	5	Legacy NDC	20241127_6cd2936e-ded7-43a2-beea-9dfaf538176f.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0316-2072-45	00316207245	148 mL in 1 TUBE (0316-2072-45)	148 ml	2021-02-09	0000-00-00	No	No	Current