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United States · US · US:0220-1249_1ddc948e-9df3-e8f9-e063-6394a90a98e4

Chamomilla

SPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBoiron
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0220124941
    12 [hp_C] in 1 TUBE (0220-1249-41)

Annotations

DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": "ORAL",
  "spl_meta": {
    "4d7af784-9f92-0dd5-e063-6394a90ab33b": {
      "match": "brand_token",
      "title": "CHAMOMILLA DEC CUPRO CULTA 3X LIQUID [URIEL PHARMACY, INC]",
      "spl_version": "1",
      "published_date": "2026-03-23"
    }
  },
  "productid": "0220-1249_1ddc948e-9df3-e8f9-e063-6394a90a98e4",
  "productndc": "0220-1249",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MATRICARIA CHAMOMILLA",
  "proprietary_name": "Chamomilla",
  "active_ingred_unit": "[hp_C]/12[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "MATRICARIA CHAMOMILLA",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "12"
}

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