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United States · US · US:64141-013_47ed81a9-35df-8d7a-e063-6394a90a77b5

BOBBI BROWN SKIN FOUNDATION

UNIISPLATC D02BA

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBobbi Brown Professional Cosmetics Inc.
CountryUS (United States)
ATC codeD02BA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6414101301
    1 BOTTLE in 1 CARTON (64141-013-01) / 30 mL in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "4Y5P7MUD51",
    "rxcui": "13369",
    "inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
    "display_name": "OCTINOXATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "a3329e11-8f1b-4e66-8b51-4ba0208612fd": {
      "match": "brand_token",
      "title": "BOBBI BROWN SKIN FOUNDATION BROAD SPECTRUM SPF 15 (OCTINOXATE AND TITANIUM DIOXIDE) LIQUID [BOBBI BROWN PROFESSIONAL COSMETICS INC.]",
      "spl_version": "12",
      "published_date": "2026-01-12"
    }
  },
  "productid": "64141-013_47ed81a9-35df-8d7a-e063-6394a90a77b5",
  "productndc": "64141-013",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTINOXATE; TITANIUM DIOXIDE",
  "proprietary_name": "BOBBI BROWN SKIN FOUNDATION",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "OCTINOXATE and TITANIUM DIOXIDE",
  "start_marketing_date": "20120901",
  "active_numerator_strength": "75; 10"
}

Related drugs

Other records sharing ATC code D02BA.

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