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United States Β· US Β· US:0220-1264_1deec84d-e13b-13c3-e063-6394a90a5c38

Chamomilla

SPL

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

Identification

ManufacturerBoiron
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    0220126441
    30 [hp_X] in 1 TUBE (0220-1264-41)

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": "0220-1264_1deec84d-e13b-13c3-e063-6394a90a5c38",
  "productndc": "0220-1264",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MATRICARIA CHAMOMILLA",
  "proprietary_name": "Chamomilla",
  "active_ingred_unit": "[hp_X]/30[hp_X]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "MATRICARIA CHAMOMILLA",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "30"
}

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Chamomilla (US) β€” Drug Database