House Dust

UNIISPL

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

Identification

ManufacturerAllermed Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
4964300805
5 mL in 1 VIAL, MULTI-DOSE (49643-008-05)
ndc11
4964300810
10 mL in 1 VIAL, MULTI-DOSE (49643-008-10)
ndc11
4964300830
30 mL in 1 VIAL, MULTI-DOSE (49643-008-30)
ndc11
4964300850
50 mL in 1 VIAL, MULTI-DOSE (49643-008-50)

Annotations

UNII (FDA Substance ID)

EYO007VX98

HOUSE DUST

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "EYO007VX98",
    "rxcui": null,
    "inchikey": null,
    "display_name": "HOUSE DUST",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "763f5534-cda1-43f2-8a37-1eaa6a43c2e8": {
      "match": "brand_token",
      "title": "HOUSE OF COLOUR TINTED SUNSCREEN SPF 50 (ZINC OXIDE) CREAM [HOUSE OF COLOUR, INC.]",
      "spl_version": "4",
      "published_date": "2026-04-20"
    }
  },
  "productid": "49643-008_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-008",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "HOUSE DUST",
  "proprietary_name": "House Dust",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "House Dust",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".02"
}

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