DR.JART EVERY SUN DAY MINERAL SUN SCREEN

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHave & Be Co., Ltd.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4940430601
1 TUBE in 1 CARTON (49404-306-01) / 50 mL in 1 TUBE

Annotations

UNII (FDA Substance ID)

15FIX9V2JP

TITANIUM DIOXIDE

RxCUI 38323

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "15FIX9V2JP",
    "rxcui": "38323",
    "inchikey": "SOQBVABWOPYFQZ-UHFFFAOYSA-N",
    "display_name": "TITANIUM DIOXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "45b1c2c6-a45b-4a45-bec9-e5341079c0a1": {
      "match": "brand_token",
      "title": "DR.JART PREMIUM BEAUTY BALM LIGHT MEDIUM-MEDIUM (ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE) CREAM [HAVE & BE CO., LTD.]",
      "spl_version": "5",
      "published_date": "2026-01-12"
    }
  },
  "productid": "49404-306_2d828e05-0be7-79cb-e063-6294a90a7716",
  "productndc": "49404-306",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "DR.JART EVERY SUN DAY MINERAL SUN SCREEN",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "titanium dioxide, zinc oxide",
  "start_marketing_date": "20230811",
  "active_numerator_strength": "41; 115"
}

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