Sunnyscreen SPF 50 Stick

Product NDC: 75936-251
Requested package NDC: 75936-251-02
11-digit product format: 759360251
Labeler code: 75936
Product ID: 75936-251_ec57b02c-991b-7bee-e053-2a95a90a20ce
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: STICK
Route: TOPICAL
Labeler: Supergoop, LLC
Application: part352
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2019-04-01
Marketing end: 0000-00-00
Substance: ZINC OXIDE
Active strength: 21 g/100g
NDC exclude flag: No
Listing certified through: 2023-12-31
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	75936-251	75936-251-02	I	Inactivated by FDA		2026-11-12

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 · 6 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
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75936-251-02	2026-01-29	C162847	48780-1	1030e365-3864-111a-e063-dadaa90a10e2	Sunnyscreen SPF 50 Stick for babies +kiddos
75936-251-02	2024-12-17	C162847	48780-1	1030e365-3864-111a-e063-dadaa90a10e2	Sunnyscreen SPF 50 Stick for babies +kiddos
75936-251-02	2024-01-30	C162847	48780-1	1030e365-3864-111a-e063-dadaa90a10e2	Sunnyscreen SPF 50 Stick for babies +kiddos

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75936-251-02	Sunnyscreen SPF 50 Stick	19.8 g in 1 TUBE	STICK	19.8		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75936-251	SUNNYSCREEN SPF 50 STICK (ZINC OXIDE) STICK [SUPERGOOP, LLC]	4	Legacy NDC, 1 package rows	20241220_857f7b28-3161-f66b-e053-2991aa0a391b.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
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
75936-251-02	75936025102	19.8 g in 1 TUBE (75936-251-02)	19.8 g	2019-04-01	0000-00-00	No	No	Current