Sunnyscreen SPF 50

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	75936-252		I	Inactivated by FDA		2026-10-05
excluded package	package	75936-252	75936-252-01	I	Inactivated by FDA		2026-10-05

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

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75936-252-01	Sunnyscreen SPF 50	100 mL in 1 BOTTLE, SPRAY	SPRAY	100		4

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75936-252	SUNNYSCREEN SPF 50 (TITANIUM DIOXIDE, ZINC OXIDE) SPRAY [SUPERGOOP, LLC]	4	Legacy NDC, 1 package rows	20241220_859461ea-582e-8185-e053-2991aa0a954a.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
75936-252-01	75936025201	100 mL in 1 BOTTLE, SPRAY (75936-252-01)	100 ml	2019-04-02	0000-00-00	No	No	Current