Salt 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
4964334505
5 mL in 1 VIAL, MULTI-DOSE (49643-345-05)
ndc11
4964334510
10 mL in 1 VIAL, MULTI-DOSE (49643-345-10)
ndc11
4964334530
30 mL in 1 VIAL, MULTI-DOSE (49643-345-30)
ndc11
4964334550
50 mL in 1 VIAL, MULTI-DOSE (49643-345-50)

Annotations

UNII (FDA Substance ID)

GOA51670YV

DISTICHLIS SPICATA POLLEN

RxCUI 852329

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "GOA51670YV",
    "rxcui": "852329",
    "inchikey": null,
    "display_name": "DISTICHLIS SPICATA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "4fae649d-f60e-0275-e063-6294a90a1ea5": {
      "match": "brand_token",
      "title": "SALT WATER VANILLA SUNSCREEN BODY BROAD SPECTRUM SPF 50 (SUNSCREEN) OIL [SALTAIR BODY LLC]",
      "spl_version": "1",
      "published_date": "2026-04-20"
    }
  },
  "productid": "49643-345_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-345",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "DISTICHLIS SPICATA POLLEN",
  "proprietary_name": "Salt Grass Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Distichlis spicata",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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