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United States · US · US:76472-3012_2ddc3214-553a-dc02-e063-6394a90a0464
Chamomilla
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSEVENE USA
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11764723012180 PELLET in 1 CYLINDER (76472-3012-1)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "SUBLINGUAL",
"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": "76472-3012_2ddc3214-553a-dc02-e063-6394a90a0464",
"productndc": "76472-3012",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MATRICARIA RECUTITA",
"proprietary_name": "Chamomilla",
"active_ingred_unit": "[kp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "MATRICARIA RECUTITA",
"start_marketing_date": "20111124",
"active_numerator_strength": "200"
}Access this data programmatically
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