Mineral Sunscreen SPF 30

Product NDC: 75936-510
11-digit product format: 759360510
Labeler code: 75936
Product ID: 75936-510_47fc0e5f-df05-b716-e063-6294a90a7656
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: SPRAY
Route: TOPICAL
Labeler: Supergoop, LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-05-15
Substance: ZINC OXIDE
Active strength: 12 g/100mL
Pharmacologic classes: Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	75936-510-01	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	75936-510-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	75936-510-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	75936-510-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	75936-510-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	75936-510-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	75936-510-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	75936-510-01	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	75936-510-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: Mineral Sunscreen SPF 30
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	12 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
SOI2LOH54Z	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4cf243b4-d794-401a-b209-18c7e550ef4f	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f47a510b-6679-4664-b2d6-47b5c4afe7cc	Product name	4	20260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120
190f2a5b-bbc8-65c7-fcb0-97891307b917	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2026-01-09	Mineral Sunscreen Mist SPF 30
2026-01-09	Mineral Sunscreen Mist SPF 30
2025-01-30	Mineral Sunscreen Mist SPF 30
2025-01-30	Mineral Sunscreen Mist SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75936-510-01	Mineral Sunscreen SPF 30	177 mL in 1 BOTTLE, SPRAY	SPRAY	177		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75936-510	MINERAL SUNSCREEN SPF 30 (ZINC OXIDE) SPRAY [SUPERGOOP, LLC]	3	Current NDC, Legacy NDC, 1 package rows	20221013_4cf243b4-d794-401a-b209-18c7e550ef4f.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 50 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ULTRALIGHT AGE DEFENSE SPF 50	ZINC OXIDE	Guangzhou Origin Beauty Cosmetics Co., Ltd.	4e36a743-7906-2b7b-e063-6294a90af314	2026-03-29	Warnings	Exact identifier application number: M020
Stay Put Sunscreen SPF 30	OCTINOXATE 7.50% OCTISALATE 5.00% OXYBENZONE 4.00% HOMOSALATE 10.00%	Sawyer Products Inc	7ecba495-a912-4697-8287-2e5836e610e1	2026-03-27	Warnings	Exact identifier application number: M020
UV SOLUTIONS BRIGHTENING TINTED BROAD SPECTRUM SPF 50 SUNSCREEN NIACINAMIDE ANTIOXIDANTS DARK SHADE	TITANIUM DIOXIDE AND ZINC OXIDE	CLINIQUE LABORATORIES LLC	4e0bd355-99c6-8cf4-e063-6294a90ab4b3	2026-03-27	Warnings	Exact identifier application number: M020
Vacation X AZ Lemon Tea Lip Balm SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Vacation INC.	61c48acc-f589-40d3-b289-b777db5551db	2026-03-27	Warnings	Exact identifier application number: M020
Truly Solar Baby Suncreen SPF 45	HOMOSALATE 15% OCTISALATE 5% OCTOCRYLENE 10% AVOBENZONE 3%	Truly Beauty, Inc	38e6c6fc-d8b9-4196-96c7-0f6d5d06da02	2026-03-26	Warnings	Exact identifier application number: M020
burnd	HOMOSALATE, OCTINOXATE, ZINC OXIDE	BURND LLC	31cf923e-fdde-790b-e063-6294a90a60ee	2026-03-26	Warnings	Exact identifier application number: M020
SUNNYSIDEKICK UVA/UVB Broad Spectrum SPF 30 Brush-On Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Classic Cosmetics LLC	4df3b8c0-71bc-acdd-e063-6394a90a35c0	2026-03-26	Warnings	Exact identifier application number: M020
COSRX	VITAMIN E VITALIZING SUNSCREEN	COSRX inc.	4df77564-9da0-7e48-e063-6294a90a5e6b	2026-03-26	Warnings	Exact identifier application number: M020
Mentholatum Natural Ice Protect Plus SPF 30 Protect Plus SPF 30	AVOBENZONE, DIMETHICONE, OCTINOXATE, OCTISALATE	The Mentholatum Company	3804a14b-be7c-a973-e063-6294a90ac7fc	2026-03-25	Warnings	Exact identifier application number: M020
Softlips Oasis Pineapple Coconut	DIMETHICONE, OXYBENZONE, OCTINOXATE	The Mentholatum Company	c504463a-28bf-4161-875f-ef73520931c5	2026-03-25	Warnings	Exact identifier application number: M020
Mentholatum Natural Ice Cherry, SPF 15 Cherry	DIMETHICONE, OCTINOXATE, OCTISALATE	The Mentholatum Company	37f2c3a6-7790-c8ec-e063-6294a90ace22	2026-03-25	Warnings	Exact identifier application number: M020
Mentholatum Natural Ice - Original, SPF 15 Original	DIMETHICONE, OCTINOXATE, OCTISALATE	The Mentholatum Company	37dc44aa-17b2-8721-e063-6294a90a34f6	2026-03-25	Warnings	Exact identifier application number: M020
ISNTREE HYALURONIC ACID DAILY SUNGEL	AVOBENZONE, HOMOSALATE, OCTISALATE	ISNTREE Inc.	0ef5d5ce-3bdf-dffc-e063-6394a90aad54	2026-03-25	Warnings	Exact identifier application number: M020
Silkscreen Sheer Tint Mineral Light-Medium	TITANIUM DIOXIDE, ZINC OXIDE	Curology	4ddbe349-6880-a5fc-e063-6294a90a275c	2026-03-25	Warnings	Exact identifier application number: M020
AXIS-Y Complete No-Stress Physical Sunscreen V.3	ZINC OXIDE	Asia Master Trade Co.,Ltd	1f310fb1-185a-b467-e063-6294a90a72fe	2026-03-25	Warnings	Exact identifier application number: M020
BANANA BOAT	TITANIUM DIOXIDE,ZINC OXIDE	Edgewell Personal Care Brands LLC	4e0450ca-147a-91d7-e063-6394a90ae73b	2026-03-25	Warnings	Exact identifier application number: M020
Mentholatum Natural Ice Original	DIMETHICONE, OCTINOXATE, OCTISALATE	The Mentholatum Company	29220eaa-87cb-4ebe-87db-d36288b3a9e4	2026-03-24	Warnings	Exact identifier application number: M020
Sport Sunscreen SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE	Amazon.com Services LLC	f54c617f-794e-413b-b898-4a06622b4bee	2026-03-24	Warnings, Adverse reactions	Exact identifier application number: M020
VITAL PERFECTION UPLIFTING AND FIRMING ADVANCED DAY	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE	Shiseido Americas Corporation	7b2d15c1-b9e1-4347-b138-9883f78822b3	2026-03-24	Warnings	Exact identifier application number: M020
Sunscreen SPF 50	SUNSCREEN SPF 50	Guangzhou Ariel Biotech Co., Ltd.	4dd05620-30a3-9cea-e063-6294a90af18b	2026-03-24	Warnings	Exact identifier application number: M020

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
75936-510-01	75936051001	177 mL in 1 BOTTLE, SPRAY (75936-510-01)	177 ml	2017-05-15	0000-00-00	No	No	Current