πΊπΈ
United States Β· US Β· US:0220-1256_1deecb05-c701-166b-e063-6394a90a402f
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
- ndc110220125641200 [kp_C] in 1 TUBE (0220-1256-41)
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": "0220-1256_1deecb05-c701-166b-e063-6394a90a402f",
"productndc": "0220-1256",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MATRICARIA CHAMOMILLA",
"proprietary_name": "Chamomilla",
"active_ingred_unit": "[kp_C]/200[kp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "MATRICARIA CHAMOMILLA",
"start_marketing_date": "19830303",
"active_numerator_strength": "200"
}Access this data programmatically
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