Nasal Dryness Relief Gel

UNIISPL

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

Identification

ManufacturerGenuine Virgin Aloe Corporation

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
1073805110
1 TUBE in 1 CARTON (10738-051-10) / 28 g in 1 TUBE (10738-051-15)

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": {
    "0ae25bc9-5d90-4dd8-9620-8684c4fd9d37": {
      "match": "brand_token",
      "title": "NASAL ALLERGY (TRIAMCINOLONE ACETONIDE) SPRAY, METERED [RUGBY LABORATORIES]",
      "spl_version": "5",
      "published_date": "2026-05-25"
    }
  },
  "productid": "10738-051_49655e27-0a67-4fca-e063-6294a90a5cfa",
  "productndc": "10738-051",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN",
  "proprietary_name": "Nasal Dryness Relief Gel",
  "active_ingred_unit": "g/100g",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Allantoin",
  "start_marketing_date": "20220520",
  "active_numerator_strength": ".5"
}

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