FDA.reportPublic FDA data

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
IngredientStrength
OCTOCRYLENE40 mg/mL
HOMOSALATE90 mg/mL
OCTINOXATE68 mg/mL
AVOBENZONE29 mg/mL
OCTISALATE45 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5A68WGF6WMInternal UNII lookup
V06SV4M95SInternal UNII lookup
4Y5P7MUD51Internal UNII lookup
G63QQF2NOXInternal UNII lookup
4X49Y0596WInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
02a72c6d-da42-14b2-e063-6394a90af5cbAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49404-307-01DR.JART EVERY SUN DAY SUN FLUID1 in 1 CARTONLIQUID13
49404-307-01DR.JART EVERY SUN DAY SUN FLUID100 mL in 1 BOTTLELIQUID1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49404-307DR.JART EVERY SUN DAY SUN FLUID (HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE) LIQUID [HAVE & BE CO., LTD.]3Current NDC, 2 package rows20250209_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 144 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Non-Tinted Foaming Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDETHE AESTHETICS ACADEMY, LLC3698c076-68b1-7d28-e063-6394a90a517c2025-12-09Exact identifier
application number: M020
Non-Tinted Replenishing Daily ProtectionZINC OXIDETHE AESTHETICS ACADEMY, LLC3699159a-3561-9ff6-e063-6394a90af9fd2025-12-09Exact identifier
application number: M020
Sheer Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDERhonda J Pomerantz MD PLLC325c1723-fb1d-ae3c-e063-6294a90a46092025-12-09Exact identifier
application number: M020
Sheer Mineral Sunscreen Satin Dewy FinishZINC OXIDETRU SKIN RITUALS3249d05b-0f5c-4787-e063-6294a90aa0d72025-12-09Exact identifier
application number: M020
Tinted Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDERhonda J Pomerantz MD PLLC325c3a18-ba8f-912d-e063-6394a90a24472025-12-09Exact identifier
application number: M020
Tinted Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDERhonda J Pomerantz MD PLLC325c8641-1161-b8ac-e063-6394a90ae4512025-12-09Exact identifier
application number: M020
Sheer Mineral Sunscreen Silk Matte FinishTITANIUM DIOXIDE, ZINC OXIDETRU SKIN RITUALS3248eb22-1e10-2091-e063-6394a90ad3e12025-12-09Exact identifier
application number: M020
Tinted Lip SunscreenTITANIUM DIOXIDE, ZINC OXIDERhonda J Pomerantz MD PLLC325cce54-a885-d586-e063-6394a90a90db2025-12-09Exact identifier
application number: M020
Sheer Mineral Lip SunscreenTITANIUM DIOXIDE, ZINC OXIDETRU SKIN RITUALS324acd75-9c38-4adc-e063-6394a90afa122025-12-09Exact identifier
application number: M020
Sheer Mineral Sunscreen Satin Dewy FinishZINC OXIDETRU SKIN RITUALS324960e6-c1e7-d2b9-e063-6294a90a92ce2025-12-09Exact identifier
application number: M020
Sol Purpose Mineral Sunscreen TintedZINC OXIDETRU SKIN RITUALS324a3475-07f0-033c-e063-6394a90a811a2025-12-09Exact identifier
application number: M020
Perfect Sunscreen SPF 50 Sheer MineralZINC OXIDEBluemercury, Inc.d8f483ff-b990-40c5-b5b8-00065051ae7e2025-12-09WarningsExact identifier
application number: M020
Foto Facial Age Delay Non-TintedTITANIUM DIOXIDE ZINC OXIDEADVANCED AESTHETIC DERMATOLOGY42674013-fa2b-42d7-e063-6294a90af9992025-12-09WarningsExact identifier
application number: M020
Hydraboost Moisturizer SPF 30AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENEBluemercuryeca867e6-4deb-4be2-ae3f-6850fb6223b32025-12-09WarningsExact identifier
application number: M020
Foto Facial Age Delay Matte TintedTITANIUM DIOXIDE ZINC OXIDEADVANCED AESTHETIC DERMATOLOGY42761919-8ae2-3c41-e063-6394a90abb8f2025-12-09WarningsExact identifier
application number: M020
Dew MineralZINC OXIDEADVANCED AESTHETIC DERMATOLOGY42f17245-92a9-3915-e063-6394a90a68172025-12-09WarningsExact identifier
application number: M020
Mineral Sunscreen Non-TintedTITANIUM DIOXIDE, ZINC OXIDEYUMA ACNE CLINIC, L.L.C.3c69b707-07ff-1a82-e063-6394a90a9fcd2025-12-09WarningsExact identifier
application number: M020
Mineral Sunscreen TintedTITANIUM DIOXIDE, ZINC OXIDEYUMA ACNE CLINIC, L.L.C.3c69f93f-0385-365c-e063-6394a90a12fd2025-12-09WarningsExact identifier
application number: M020
Replenishing Daily Protection TintedZINC OXIDEYUMA ACNE CLINIC, L.L.C.3c6a5601-a7a2-5e20-e063-6394a90a66432025-12-09WarningsExact identifier
application number: M020
Bronzing Blendrops Broad Spectrum SPF 40HOMOSALATE, OCTISALATE, ZINC OXIDEWasatch Product Development, LLC124ca946-8412-4d6d-e063-6294a90a63382025-12-09WarningsExact identifier
application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49404-307-01494040307011 BOTTLE in 1 CARTON (49404-307-01) / 100 mL in 1 BOTTLE1 bottle2023-08-112027-11-30NoNoHistorical