Velvet Grass Pollen

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
4964336105
5 mL in 1 VIAL, MULTI-DOSE (49643-361-05)
ndc11
4964336110
10 mL in 1 VIAL, MULTI-DOSE (49643-361-10)
ndc11
4964336130
30 mL in 1 VIAL, MULTI-DOSE (49643-361-30)
ndc11
4964336150
50 mL in 1 VIAL, MULTI-DOSE (49643-361-50)

Annotations

UNII (FDA Substance ID)

70O1TP6H01

HOLCUS LANATUS POLLEN

RxCUI 852514

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "70O1TP6H01",
    "rxcui": "852514",
    "inchikey": null,
    "display_name": "HOLCUS LANATUS POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "35a8508d-7069-c2d6-e063-6394a90a6219": {
      "match": "brand_token",
      "title": "VELVET NT MOISTURIZING MINERAL SUNSCREEN (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [SKIN BOSS L.L.C.]",
      "spl_version": "2",
      "published_date": "2025-12-16"
    }
  },
  "productid": "49643-361_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-361",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "HOLCUS LANATUS POLLEN",
  "proprietary_name": "Velvet Grass Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Holcus lanatus",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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