Dr.Jucre Rebirth Activating Toner

UNIISPLATC A16AA06

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

Identification

ManufacturerNATURECELL CO., LTD.

CountryUS (United States)

ATC codeA16AA06

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8307102002
1 BOTTLE in 1 CARTON (83071-020-02) / 150 mL in 1 BOTTLE (83071-020-01)

Annotations

UNII (FDA Substance ID)

3SCV180C9W

BETAINE

RxCUI 350374

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "3SCV180C9W",
    "rxcui": "350374",
    "inchikey": "KWIUHFFTVRNATP-UHFFFAOYSA-N",
    "display_name": "BETAINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "2ab49052-085f-024e-e063-6394a90a81b8": {
      "match": "brand_token",
      "title": "DR.JUCRE REBIRTH SUN PROTECTION (OCTINOXATE, HOMOSALATE, OCTISALATE, AVOBENZONE, ENSULIZOLE, OCTOCRYLENE, BEMOTRIZINOL, NIACINAMIDE, ADENOSINE) CREAM [NATURECELL CO., LTD.]",
      "spl_version": "1",
      "published_date": "2025-01-03"
    }
  },
  "productid": "83071-020_ff0ae282-1f6c-441a-a7dd-863b46931dc2",
  "productndc": "83071-020",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BETAINE",
  "proprietary_name": "Dr.Jucre Rebirth Activating Toner",
  "active_ingred_unit": "g/100mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Betaine",
  "start_marketing_date": "20221001",
  "active_numerator_strength": ".001"
}

Related drugs

Other records sharing ATC code A16AA06.

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