Scutellaria Lateriflora

UNIISPL

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766222771
200 PELLET in 1 VIAL, GLASS (37662-2277-1)
ndc11
3766222772
500 PELLET in 1 VIAL, GLASS (37662-2277-2)
ndc11
3766222773
3000 PELLET in 1 BOTTLE, GLASS (37662-2277-3)
ndc11
3766222774
10000 PELLET in 1 BOTTLE, GLASS (37662-2277-4)

Annotations

UNII (FDA Substance ID)

7BP4DH5PDC

SCUTELLARIA LATERIFLORA WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "7BP4DH5PDC",
    "rxcui": null,
    "inchikey": null,
    "display_name": "SCUTELLARIA LATERIFLORA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3a88b661-0b82-6225-e063-6394a90a18e7": {
      "match": "brand_token",
      "title": "SCUTELLARIA LATERIFLORA (SCUTELLARIA LATERIFLORA WHOLE) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-20"
    }
  },
  "productid": "37662-2277_f1dd6d9b-f1d8-0820-e053-2a95a90a82a6",
  "productndc": "37662-2277",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SCUTELLARIA LATERIFLORA WHOLE",
  "proprietary_name": "Scutellaria Lateriflora",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Scutellaria Lateriflora",
  "start_marketing_date": "20230109",
  "active_numerator_strength": "10"
}

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