Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen

UNIISPL

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

Identification

ManufacturerL'Oreal USA Products Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4996759501
150 mL in 1 BOTTLE, PLASTIC (49967-595-01)

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": {
    "22e088b9-b3b1-4c34-be12-a5a31200ec25": {
      "match": "brand_token",
      "title": "KIEHLS SINCE 1851 ULTRA FACIAL MELTDOWN RECOVERY (COLLOIDAL OATMEAL) CREAM [L&RSQUO;OREAL USA PRODUCTS INC]",
      "spl_version": "8",
      "published_date": "2026-06-01"
    }
  },
  "productid": "49967-595_676f1412-f75f-4dc4-a76a-57c360aeb54c",
  "productndc": "49967-595",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE",
  "proprietary_name": "Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium dioxide",
  "start_marketing_date": "20130601",
  "active_numerator_strength": "110"
}

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