DR.JART EVERY SUN DAY MINERAL SUN SCREEN

Product NDC: 49404-306
11-digit product format: 494040306
Labeler code: 49404
Product ID: 49404-306_2d828e05-0be7-79cb-e063-6294a90a7716
Type: HUMAN OTC DRUG
Nonproprietary name: titanium dioxide, zinc oxide
Dosage form: CREAM
Route: TOPICAL
Labeler: Have & Be Co., Ltd.
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-08-11
Marketing end: 2027-12-31
Substance: TITANIUM DIOXIDE; ZINC OXIDE
Active strength: 41; 115 mg/mL; mg/mL
NDC exclude flag: No
Current FDA listing: Yes

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	49404-306	49404-306-02	D	Discontinued by firm		2026-11-13

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
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…`

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: DR.JART EVERY SUN DAY MINERAL SUN SCREEN

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TITANIUM DIOXIDE	41 mg/mL
ZINC OXIDE	115 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
15FIX9V2JP	Internal UNII lookup
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
02a671ed-485d-d6b7-e063-6394a90ad4af	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
49404-306-01	DR.JART EVERY SUN DAY MINERAL SUN SCREEN	50 mL in 1 TUBE	CREAM	50	4
49404-306-01	DR.JART EVERY SUN DAY MINERAL SUN SCREEN	1 in 1 CARTON	CREAM	1	4
49404-306-02	DR.JART EVERY SUN DAY MINERAL SUN SCREEN	5 mL in 1 TUBE	CREAM	5	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49404-306	DR.JART EVERY SUN DAY MINERAL SUN SCREEN (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [HAVE & BE CO., LTD.]	4	Current NDC, 3 package rows	20250209_02a671ed-485d-d6b7-e063-6394a90ad4af.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 252 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Fresh Coast SPF 50 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	043cadde-ba07-7c77-e063-6394a90abee6	2024-12-19	Warnings	Exact identifier application number: M020
Black Girl Sunscreen SPF 30	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 8%	Derma Care Research Labs, LLC	d438be95-0f88-69d7-e053-2995a90a982e	2024-12-19	Warnings	Exact identifier application number: M020
Pavin SPF 50 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	e945f9df-0aed-469c-e053-2995a90ab6aa	2024-12-19	Warnings	Exact identifier application number: M020
Bee Bald Smooth Plus Daily Moisturizer SPF 30 Sunscreen	AVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 2.7%, OXYBENZONE 6%	Derma Care Research Labs, LLC	051b68f9-5d6b-3cd7-e063-6394a90aeb35	2024-12-19	Warnings	Exact identifier application number: M020
MKMen Advanced Facial Hydrator Sunscreen SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	Mary Kay Inc.	484e92db-09a2-4e93-aa7e-d91dbda31555	2024-12-19	Warnings	Exact identifier application number: M020
SPF 50 Sunscreen Unfragranced	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	05e4706b-1955-aba8-e063-6294a90a29c7	2024-12-19	Warnings	Exact identifier application number: M020
Rubber Ducky SPF 50 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	cf32b3a0-de88-b866-e053-2a95a90a3f32	2024-12-19	Warnings	Exact identifier application number: M020
SPF 50 Sunscreen Rocky Mountain	AVOBENZONE 3%, HOMOSALATE 10%, OCTOCRYLENE 6%	Derma Care Research Labs, LLC	a216d48f-4ed4-6008-e053-2a95a90a8c9a	2024-12-19	Warnings	Exact identifier application number: M020
Rod and Rifle SPF 50 Sunscreen	AVOBENZONE 3%, HOMOSALATE 10%, OCTOCRYLENE 6%	Derma Care Research Labs, LLC	fc61847b-cb61-97b1-e053-6394a90ae1b9	2024-12-19	Warnings	Exact identifier application number: M020
Habana Brisa SPF 30 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 6%	Derma Care Research Labs, LLC	db0d6dec-d0ee-6160-e053-2a95a90a2c6e	2024-12-19	Warnings	Exact identifier application number: M020
Caribbean Breeze SPF 30 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 8%	Derma Care Research Labs, LLC	f8730f9c-43c1-f4d3-e053-6294a90a1809	2024-12-19	Warnings	Exact identifier application number: M020
Caribbean Breeze SPF 50 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	f8735925-dcb2-6723-e053-6294a90a51f4	2024-12-19	Warnings	Exact identifier application number: M020
Caribbean Breeze SPF 70 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	f873c125-86b8-3d1d-e053-6394a90a6bcf	2024-12-19	Warnings	Exact identifier application number: M020
Royal Boost Cover Me Sunscreen Broad Spectrum SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Distribuidora Comercial Jafra, S.A. de C.V.	efd7d887-0616-4c76-84d8-5370eb63cb7f	2024-12-19	Warnings	Exact identifier application number: M020
Rubber Ducky SPF 50 Unfragranced Sunscreen	AVOBENZONE 3%, HOMOSALATE 10%, OCTOCRYLENE 6%	Derma Care Research Labs, LLC	043b447c-4519-37ce-e063-6394a90a7197	2024-12-19	Warnings	Exact identifier application number: M020
Australian Sands SPF 50 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	f886a02f-c043-b281-e053-6294a90af746	2024-12-19	Warnings	Exact identifier application number: M020
SPF 50 Sunscreen Rocky Mountain	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	a1c9066c-4801-5aee-e053-2995a90a75d2	2024-12-19	Warnings	Exact identifier application number: M020
Dr. Throwers SPF 30 Face and Body Sunscreen	AVOBENZONE 3%, HOMOSALATE 12%, OCTISALATE 5%, OCTOCRYLENE 3%	Derma Care Research Labs, LLC	d680b6f6-e1a9-47a4-e053-2a95a90ae3b0	2024-12-19	Warnings	Exact identifier application number: M020
Vacation Broad Spectrum SPF 30	HOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE	Vacation Inc.	29a7636c-4d99-2cac-e063-6394a90a7480	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 CARAMEL	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29a82ba9-c0f8-0edf-e063-6294a90a50b4	2024-12-19	Warnings	Exact identifier application number: M020

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49404-306-01	49404030601	1 TUBE in 1 CARTON (49404-306-01) / 50 mL in 1 TUBE	1 tube	2023-08-11	2027-12-31	No	No	Historical
49404-306-02	49404030602	5 mL in 1 TUBE	5 ml					Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
DR.JART EVERY SUN DAY MINERAL SUN SCREEN	Have & Be Co., Ltd. \| Estee Lauder Companies Inc. \| HK Kolmar Canada, Inc	2025-02-06	HUMAN OTC DRUG LABEL	4