DR.JART EVERY SUN DAY SUN FLUID

Product NDC: 49404-307
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 253 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SABLE	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29a8812b-70ff-e8aa-e063-6294a90a09f8	2024-12-19	Warnings	Exact identifier application number: M020
CLE CCC Neutral Deep	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, AVOBENZONE	KW ABSC, INC.	3a548deb-3670-4c5b-a139-796701801fed	2024-12-19	Warnings	Exact identifier application number: M020
CLE CCC Olive Medium Deep	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	be4434c0-cbdd-46cb-8015-4c7859e80d4a	2024-12-19	Warnings	Exact identifier application number: M020
CLE CCC Golden Medium	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	de50e956-a014-4147-922b-63c95fa6f86b	2024-12-19	Warnings	Exact identifier application number: M020
CLE CCC Neutral Light	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	44cbb226-83ed-401b-baf8-ca8e4740dbef	2024-12-19	Warnings	Exact identifier application number: M020
CLE CCC Neutral Medium Light	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	615f5e39-695d-41d4-af59-e0d3b76789bb	2024-12-19	Warnings	Exact identifier application number: M020
CLE CCC Warm Deep	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, AVOBENZONE	KW ABSC, INC.	6ab3e360-8104-4439-93fb-e11bc4a77558	2024-12-19	Warnings	Exact identifier application number: M020
CLE CCC Neutral Medium	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	a297ff64-678c-4936-8384-022606a2f33c	2024-12-19	Warnings	Exact identifier application number: M020
CLE CCC Neutral Fair	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	aa8176c6-f1c9-43dd-96e0-f7d6ed30a1a2	2024-12-19	Warnings	Exact identifier application number: M020
CLE CCC Cool Medium Deep	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	2e0365f9-d3c6-4404-90ac-772a829b3ade	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18- D2 NUTMEG	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29abae8f-53db-b592-e063-6294a90adabb	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 MOCHA	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29aba80c-55b7-b8d9-e063-6294a90a5cc1	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 COCOA	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29abe97b-e9b3-6e27-e063-6294a90ae3ed	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 DEEP GOLDEN	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29abdf3c-fb54-a5e3-e063-6394a90af450	2024-12-19	Warnings	Exact identifier application number: M020
MILK TINT SPF 43 TINTED PRIMER SERUM FAIR	ZINC OXIDE	COSMAX USA, CORPORATION	29ac756b-3df7-50c9-e063-6394a90aa479	2024-12-19	Warnings	Exact identifier application number: M020
MILK TINT SPF 43 TINTED PRIMER SERUM RICH	ZINC OXIDE	COSMAX USA, CORPORATION	29ac51a0-07e7-ad7b-e063-6294a90ae777	2024-12-19	Warnings	Exact identifier application number: M020
MILK TINT SPF 43 TINTED PRIMER SERUM DEEPEST	ZINC OXIDE	COSMAX USA, CORPORATION	29ad12e2-0a2e-7138-e063-6394a90aebaf	2024-12-19	Warnings	Exact identifier application number: M020
CeraVe Developed with Dermatologists Hydrating Mineral Sunscreen Broad Spectrum SPF 30 Face Sheer Tint Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	L'Oreal USA Products, Inc.	f2e34230-7bfb-455f-8b33-6bff96fd9f0a	2024-12-19	Warnings	Exact identifier application number: M020
Anew Platinum DayCream Broad Spectrum SPF 25	AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE	COSMAX USA, CORPORATION	56200212-bedc-6e1e-e063-6394a90a3666	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SHELL	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29868d60-b900-e0ad-e063-6294a90af87a	2024-12-18	Warnings	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