KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery

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 · 6

ndc11
4996757101
1 TUBE in 1 CARTON (49967-571-01) / 14 mL in 1 TUBE
ndc11
4996757102
28 mL in 1 JAR (49967-571-02)
ndc11
4996757103
50 mL in 1 JAR (49967-571-03)
ndc11
4996757104
3 mL in 1 PACKET (49967-571-04)
ndc11
4996757105
125 mL in 1 JAR (49967-571-05)
ndc11
4996757106
150 mL in 1 POUCH (49967-571-06)

Annotations

UNII (FDA Substance ID)

8PI54V663Y

OATMEAL

RxCUI 221082

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "8PI54V663Y",
    "rxcui": "221082",
    "inchikey": null,
    "display_name": "OATMEAL",
    "substance_type": "structurallyDiverse",
    "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": "49967-571_52f75c0f-c209-9fcb-e063-6294a90a1eae",
  "productndc": "49967-571",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OATMEAL",
  "proprietary_name": "KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery",
  "active_ingred_unit": "mg/mL",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Colloidal oatmeal",
  "start_marketing_date": "20251115",
  "active_numerator_strength": "10"
}

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