Vanilla Planifolia

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
3766232261
200 PELLET in 1 VIAL, GLASS (37662-3226-1)
ndc11
3766232262
500 PELLET in 1 VIAL, GLASS (37662-3226-2)
ndc11
3766232263
3000 PELLET in 1 BOTTLE, GLASS (37662-3226-3)
ndc11
3766232264
10000 PELLET in 1 BOTTLE, GLASS (37662-3226-4)

Annotations

UNII (FDA Substance ID)

Q74T35078H

VANILLA BEAN

RxCUI 901291

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "Q74T35078H",
    "rxcui": "901291",
    "inchikey": null,
    "display_name": "VANILLA BEAN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "5228794d-0048-bb6d-e063-6394a90acdae": {
      "match": "brand_token",
      "title": "VANILLA SALT AIR HAND SANITIZER (ETHYL ALCOHOL) LIQUID [PEACH LAYNE, LLC]",
      "spl_version": "1",
      "published_date": "2026-06-02"
    }
  },
  "productid": "37662-3226_fc636b53-c038-2fef-e053-6394a90aaca6",
  "productndc": "37662-3226",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "VANILLA BEAN",
  "proprietary_name": "Vanilla Planifolia",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Vanilla Planifolia",
  "start_marketing_date": "20230523",
  "active_numerator_strength": "200"
}

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