OrgaPlus Super Care Balm for combination and oi ly skin type

UNIISPL

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

Identification

ManufacturerBLUEZONWIDE CO.,LTD

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6977719002
1 CONTAINER in 1 CARTON (69777-190-02) / 20 g in 1 CONTAINER (69777-190-01)

Annotations

UNII (FDA Substance ID)

3W1JG795YI

SUNFLOWER OIL

RxCUI 37422

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "3W1JG795YI",
    "rxcui": "37422",
    "inchikey": null,
    "display_name": "SUNFLOWER OIL",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "d3c422f6-a83d-48fc-94fc-2749666426c8": {
      "match": "brand_token",
      "title": "ORGAPLUS ULTRA PURE SUN EX 22G (OCTINOXATE, OCTISALATE, OCTOCRYLENE) STICK [BLUEZONWIDE CO.,LTD]",
      "spl_version": "2",
      "published_date": "2025-02-06"
    }
  },
  "productid": "69777-190_2d5fef46-0c05-5058-e063-6294a90a06c1",
  "productndc": "69777-190",
  "dosage_form": "STICK",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SUNFLOWER OIL",
  "proprietary_name": "OrgaPlus Super Care Balm for combination and oi ly skin type",
  "active_ingred_unit": "g/20g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "SUNFLOWER",
  "start_marketing_date": "20171101",
  "active_numerator_strength": "11.31"
}

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