Kinfield Relief Balm Anti-Itch Remedy

UNIISPL

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

Identification

ManufacturerKinfield, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
8175002017
1 TUBE in 1 PACKAGE (81750-020-17) / 17 g in 1 TUBE
ndc11
8175002040
1 TUBE in 1 PACKAGE (81750-020-40) / 40 g in 1 TUBE

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": {
    "cbdfd0ae-514b-4b53-98ad-4270163bd0df": {
      "match": "brand_token",
      "title": "KINFIELD SUNGLOW LUMINIZING FACIAL SUNSCREEN BROAD SPECTRUM SPF 35 LOTION [KINFIELD, INC.]",
      "spl_version": "5",
      "published_date": "2025-12-31"
    }
  },
  "productid": "81750-020_472bacf4-c61c-8f20-e063-6294a90a360b",
  "productndc": "81750-020",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OATMEAL",
  "proprietary_name": "Kinfield Relief Balm Anti-Itch Remedy",
  "active_ingred_unit": "g/17g",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Kinfield Relief Balm Anti-Itch Remedy",
  "start_marketing_date": "20210405",
  "active_numerator_strength": "10"
}

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