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United States · US · US:49967-410_fce707d4-51c3-486f-82fa-eb80d11498f6

Kiehls Since 1851 Super Multi Corrective Broad Spectrum SPF 30 Sunscreen

UNIISPL

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

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 · 4

  • ndc11
    4996741001
    50 mL in 1 JAR (49967-410-01)
  • ndc11
    4996741002
    125 mL in 1 JAR (49967-410-02)
  • ndc11
    4996741003
    75 mL in 1 JAR (49967-410-03)
  • ndc11
    4996741004
    3 mL in 1 PACKET (49967-410-04)

Annotations

UNII (FDA Substance ID)
G63QQF2NOX
AVOBENZONE
RxCUI 45045
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "G63QQF2NOX",
    "rxcui": "45045",
    "inchikey": "XNEFYCZVKIDDMS-UHFFFAOYSA-N",
    "display_name": "AVOBENZONE",
    "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’OREAL USA PRODUCTS INC]",
      "spl_version": "8",
      "published_date": "2026-06-01"
    }
  },
  "productid": "49967-410_fce707d4-51c3-486f-82fa-eb80d11498f6",
  "productndc": "49967-410",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "Kiehls Since 1851 Super Multi Corrective Broad Spectrum SPF 30 Sunscreen",
  "active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Avobenzone, Homosalate, Octisalate and Octocrylene",
  "start_marketing_date": "20150701",
  "active_numerator_strength": "30; 50; 50; 70"
}

Access this data programmatically

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