ARC Skin Protectant

UNIISPL

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

Identification

ManufacturerAnjon Biologics, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
6914800101
60 g in 1 TUBE (69148-001-01)
ndc11
6914800102
100 g in 1 TUBE (69148-001-02)

Annotations

UNII (FDA Substance ID)

344S277G0Z

ALLANTOIN

RxCUI 508

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "344S277G0Z",
    "rxcui": "508",
    "inchikey": "POJWUDADGALRAB-UHFFFAOYSA-N",
    "display_name": "ALLANTOIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "12634efa-35e3-76d7-e063-6294a90a3de4": {
      "match": "brand_token",
      "title": "ARC 2 IN 1 WHITENING AND ANTICAVITY (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY]",
      "spl_version": "5",
      "published_date": "2026-01-12"
    }
  },
  "productid": "69148-001_8b450573-d048-4077-8c0b-9e0a2e8a72c2",
  "productndc": "69148-001",
  "dosage_form": "OINTMENT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN",
  "proprietary_name": "ARC Skin Protectant",
  "active_ingred_unit": "g/100g",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ALLANTOIN",
  "start_marketing_date": "20140806",
  "active_numerator_strength": ".5"
}

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