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 |
|---|---|
| OCTOCRYLENE | 40 mg/mL |
| HOMOSALATE | 90 mg/mL |
| OCTINOXATE | 68 mg/mL |
| AVOBENZONE | 29 mg/mL |
| OCTISALATE | 45 mg/mL |
Harmonized UNII identifiers#
| 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#
| Identifier | FDA.report destination |
|---|---|
| 02a72c6d-da42-14b2-e063-6394a90af5cb | Available on FDA.report |
DailyMed Product Concepts#
| 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 | 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#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Safe Sea SPF sport 65 | HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE | NIDARIA TECHNOLOGY LTD | 0ed3242b-ac35-4d98-a777-1e44bb32a467 | 2025-12-08 | Warnings | M020 |
| Safe Sea SPF 50 | HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE | NIDARIA TECHNOLOGY LTD | 46641a33-d658-4ef0-9b7a-062adc401dde | 2025-12-08 | Warnings | M020 |
| Skin Filter Glow SPF | ZINC OXIDE | MALORIE MILES | 36485f44-a6bd-9529-e063-6294a90af7a4 | 2025-12-08 | M020 | |
| Skin Filter Matte SPF | TITANIUM DIOXIDE, ZINC OXIDE | MALORIE MILES | 3647f983-9e75-8955-e063-6294a90af162 | 2025-12-08 | M020 | |
| Body-Screen | ZINC OXIDE | MALORIE MILES | 36499be5-d680-92bf-e063-6394a90a89db | 2025-12-08 | M020 | |
| Skin Filter Matte SPF | TITANIUM DIOXIDE, ZINC OXIDE | MALORIE MILES | 3649f758-e31b-3c6a-e063-6294a90a5c36 | 2025-12-08 | M020 | |
| Body-Screen | ZINC OXIDE | MALORIE MILES | 364ae392-480a-14ea-e063-6394a90a3883 | 2025-12-08 | M020 | |
| Personalized Moisturizer SPF 30 | ZINC OXIDE 10.00% | Proven Skincare | d3cf8f81-d6ae-4570-ad86-43415e973e13 | 2025-12-08 | Warnings | M020 |
| GLOW SHIELD SPF | ZINC OXIDE | ACNE SOLUTIONS NYC INC | 2f9d087c-b2b3-5654-e063-6294a90a94e5 | 2025-12-08 | Warnings | M020 |
| MATTE SHIELD SPF | ZINC OXIDE | ACNE SOLUTIONS NYC INC | 2faee7ef-fc0c-6d01-e063-6294a90a6d68 | 2025-12-08 | Warnings | M020 |
| GLOW SHIELD SPF | ZINC OXIDE | ACNE SOLUTIONS NYC INC | 2faf530d-5574-b702-e063-6294a90ad6fd | 2025-12-08 | Warnings | M020 |
| MATTE SHIELD SPF | ZINC OXIDE | ACNE SOLUTIONS NYC INC | 2fb00db0-4c37-56c6-e063-6294a90a8aff | 2025-12-08 | Warnings | M020 |
| Matte Shield SPF | TITANIUM DIOXIDE, ZINC OXIDE | ACNE SOLUTIONS NYC INC | 3bb582ec-71e7-4ad8-e063-6394a90a94d4 | 2025-12-08 | Warnings | M020 |
| SPF 101 Lightly Tinted | ZINC OXIDE | The Acne Lab LLC | 334afdc8-1e12-d787-e063-6294a90aed7c | 2025-12-08 | M020 | |
| SPF 101 Non-Tinted | ZINC OXIDE | The Acne Lab LLC | 334bf8ea-2485-84e8-e063-6294a90aefa6 | 2025-12-08 | M020 | |
| SPF 101 Lightly Tinted | ZINC OXIDE | The Acne Lab LLC | 334d694a-f9e4-ae86-e063-6394a90abfe1 | 2025-12-08 | M020 | |
| SPF 101 Non-Tinted | ZINC OXIDE | The Acne Lab LLC | 334e32a4-c3a5-e37d-e063-6294a90ad6cf | 2025-12-08 | M020 | |
| Mineral Based Sunscreen Stick Non-Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 3245561d-a90c-7bf0-e063-6394a90ab3b6 | 2025-12-08 | M020 | |
| Mineral Based Sunscreen Stick Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 3245c1f7-2c1b-b6ad-e063-6394a90aaee6 | 2025-12-08 | M020 | |
| Mineral Based Facial Sunscreen | ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 3e8981ed-5847-7009-e063-6394a90a49a1 | 2025-12-08 | Warnings | M020 |
Packages#
| 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 |