DR.JART EVERY SUN DAY SUN FLUID

Product NDC: 49404-307
Requested package NDC: 49404-307-01
11-digit product format: 494040307
Labeler code: 49404
Product ID: 49404-307_2d82a7ff-8d4d-02d2-e063-6394a90a2347
Type: HUMAN OTC DRUG
Nonproprietary name: homosalate, octinoxate, octisalate, octocrylene, avobenzone
Dosage form: LIQUID
Route: TOPICAL
Labeler: Have & Be Co., Ltd.
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-08-11
Marketing end: 2027-11-30
Substance: OCTOCRYLENE; HOMOSALATE; OCTINOXATE; AVOBENZONE; OCTISALATE
Active strength: 40; 90; 68; 29; 45 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag: No
Current FDA listing: Yes

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 SUN FLUID

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTOCRYLENE	40 mg/mL
HOMOSALATE	90 mg/mL
OCTINOXATE	68 mg/mL
AVOBENZONE	29 mg/mL
OCTISALATE	45 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5A68WGF6WM	Internal UNII lookup
V06SV4M95S	Internal UNII lookup
4Y5P7MUD51	Internal UNII lookup
G63QQF2NOX	Internal UNII lookup
4X49Y0596W	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
02a72c6d-da42-14b2-e063-6394a90af5cb	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
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49404-307-01	DR.JART EVERY SUN DAY SUN FLUID	1 in 1 CARTON	LIQUID	1		3
49404-307-01	DR.JART EVERY SUN DAY SUN FLUID	100 mL in 1 BOTTLE	LIQUID	100		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49404-307	DR.JART EVERY SUN DAY SUN FLUID (HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE) LIQUID [HAVE & BE CO., LTD.]	3	Current NDC, 2 package rows	20250209_02a72c6d-da42-14b2-e063-6394a90af5cb.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 115 of 353 · 7,041 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Non Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	JEFFREY J. ROTH, M.D., A PROFESSIONAL CORPORATION	36c00301-ee41-333c-e063-6294a90a61d5	2025-12-16		Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	JEFFREY J. ROTH, M.D., A PROFESSIONAL CORPORATION	36c078fa-05f9-ad80-e063-6394a90af3bb	2025-12-16		Exact identifier application number: M020
20Percent Zinc Oxide Non Tinted	ZINC OXIDE	JEFFREY J. ROTH, M.D., A PROFESSIONAL CORPORATION	36c108f6-a928-0a54-e063-6394a90ae686	2025-12-16		Exact identifier application number: M020
20Percent Zinc Oxide Non Tinted	ZINC OXIDE	JEFFREY J. ROTH, M.D., A PROFESSIONAL CORPORATION	36c0ccca-c993-181e-e063-6294a90a7ae6	2025-12-16		Exact identifier application number: M020
Non Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	JEFFREY J. ROTH, M.D., A PROFESSIONAL CORPORATION	36c0a55d-16d3-086a-e063-6394a90a30cf	2025-12-16		Exact identifier application number: M020
Eucerin Radiant Tone	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Beiersdorf Inc	2611e0cb-d56d-6ea1-e063-6294a90a745b	2025-12-16	Warnings	Exact identifier application number: M020
Really Great Lip Shield	TITANIUM DIOXIDE, ZINC OXIDE	JEFFREY J. ROTH, M.D., A PROFESSIONAL CORPORATION	36c1341d-fbf5-56a5-e063-6294a90aa045	2025-12-16		Exact identifier application number: M020
Tinted Mineral Sunscreen	ZINC OXIDE	KLOE SALON LLC	36c23c07-2011-3ddb-e063-6294a90a76e9	2025-12-16		Exact identifier application number: M020
Tinted Mineral Sun Defense	TITANIUM DIOXIDE, ZINC OXIDE	Helen's Haven	36c465ea-979b-9474-e063-6394a90ab3f8	2025-12-16		Exact identifier application number: M020
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Helen's Haven	36c4a27b-96e9-4f30-e063-6294a90a5655	2025-12-16		Exact identifier application number: M020
Mineral Sunscreen Non Tinted	TITANIUM DIOXIDE, ZINC OXIDE	SAN JOSE MEDICAL SPA	37ef19e5-1775-a8d5-e063-6394a90acaef	2025-12-16		Exact identifier application number: M020
Tinted Mineral Sunscreen	ZINC OXIDE, TITANIUM DIOXIDE	BABYFACE LLC	36d69eb5-59b4-14a0-e063-6394a90a0a49	2025-12-16		Exact identifier application number: M020
Non Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	BABYFACE LLC	36d6141c-6967-d779-e063-6294a90af0a7	2025-12-16		Exact identifier application number: M020
Replenishing Daily Sunscreen	ZINC OXIDE	BABYFACE LLC	36d773d7-349d-68c1-e063-6394a90aff1e	2025-12-16		Exact identifier application number: M020
TiZO Tinted Moisturizing Serum - Light	ZINC OXIDE	Fallien Cosmeceuticals, Ltd.	2d44158a-44b3-5a3d-e063-6294a90a1f16	2025-12-16	Warnings	Exact identifier application number: M020
TiZO Tinted Moisturizing Serum - Light-Medium	ZINC OXIDE	Fallien Cosmeceuticals, Ltd.	2d53071f-0275-d00c-e063-6294a90afcca	2025-12-16	Warnings	Exact identifier application number: M020
TiZO Tinted Moisturizing Serum - Medium	ZINC OXIDE	Fallien Cosmeceuticals, Ltd.	2d550967-25af-3e7a-e063-6394a90a2c79	2025-12-16	Warnings	Exact identifier application number: M020
TiZO Tinted Moisturizing Serum - Medium-Deep	ZINC OXIDE	Fallien Cosmeceuticals, Ltd.	2d57790c-22cf-08aa-e063-6394a90aeac0	2025-12-16	Warnings	Exact identifier application number: M020
TiZO Tinted Moisturizing Serum - Deep	ZINC OXIDE	Fallien Cosmeceuticals, Ltd.	2d5813e8-a219-db90-e063-6294a90a6ca7	2025-12-16	Warnings	Exact identifier application number: M020
Non-Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	ESTHETIC ACADEMY LLC	36c043e0-fd6c-5f7a-e063-6294a90a8899	2025-12-16		Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49404-307-01	49404030701	1 BOTTLE in 1 CARTON (49404-307-01) / 100 mL in 1 BOTTLE	1 bottle	2023-08-11	2027-11-30	No	No	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
DR.JART EVERY SUN DAY SUN FLUID	Have & Be Co., Ltd. \| Estee Lauder Companies Inc. \| HK Kolmar Canada, Inc	2025-02-06	HUMAN OTC DRUG LABEL	3