dr.jart every sun day sun fluid

Generic: homosalate, octinoxate, octisalate, octocrylene, avobenzone

Labeler: have & be co., ltd.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dr.jart every sun day sun fluid
Generic Name homosalate, octinoxate, octisalate, octocrylene, avobenzone
Labeler have & be co., ltd.
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

avobenzone 29 mg/mL, homosalate 90 mg/mL, octinoxate 68 mg/mL, octisalate 45 mg/mL, octocrylene 40 mg/mL

Manufacturer
Have & Be Co., Ltd.

Identifiers & Regulatory

Product NDC 49404-307
Product ID 49404-307_2d82a7ff-8d4d-02d2-e063-6394a90a2347
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Marketing Start 2023-08-11
Marketing End 2027-11-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49404307
Hyphenated Format 49404-307

Supplemental Identifiers

UPC
8809642712843
UNII
G63QQF2NOX V06SV4M95S 4Y5P7MUD51 4X49Y0596W 5A68WGF6WM

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dr.jart every sun day sun fluid (source: ndc)
Generic Name homosalate, octinoxate, octisalate, octocrylene, avobenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 29 mg/mL
  • 90 mg/mL
  • 68 mg/mL
  • 45 mg/mL
  • 40 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (49404-307-01) / 100 mL in 1 BOTTLE
source: ndc

Packages (1)

49404-307-01 1 BOTTLE in 1 CARTON (49404-307-01) / 100 mL in 1 BOTTLE

Ingredients (5)

avobenzone (29 mg/mL) homosalate (90 mg/mL) octinoxate (68 mg/mL) octisalate (45 mg/mL) octocrylene (40 mg/mL)

Linked Drug Pages (1)

DR.JART EVERY SUN DAY SUN FLUID ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2d82a7ff-8d4d-02d2-e063-6394a90a2347", "openfda": {"upc": ["8809642712843"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4Y5P7MUD51", "4X49Y0596W", "5A68WGF6WM"], "spl_set_id": ["02a72c6d-da42-14b2-e063-6394a90af5cb"], "manufacturer_name": ["Have & Be Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49404-307-01)  / 100 mL in 1 BOTTLE", "package_ndc": "49404-307-01", "marketing_end_date": "20271130", "marketing_start_date": "20230811"}], "brand_name": "DR.JART EVERY SUN DAY SUN FLUID", "product_id": "49404-307_2d82a7ff-8d4d-02d2-e063-6394a90a2347", "dosage_form": "LIQUID", "product_ndc": "49404-307", "generic_name": "homosalate, octinoxate, octisalate, octocrylene, avobenzone", "labeler_name": "Have & Be Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DR.JART EVERY SUN DAY SUN FLUID", "active_ingredients": [{"name": "AVOBENZONE", "strength": "29 mg/mL"}, {"name": "HOMOSALATE", "strength": "90 mg/mL"}, {"name": "OCTINOXATE", "strength": "68 mg/mL"}, {"name": "OCTISALATE", "strength": "45 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "40 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20271130", "marketing_start_date": "20230811"}