Chamomilla Dec Cupro culta 3X

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Chamomilla Dec Cupro culta 3X
Generic name: CHAMOMILLA DEC CUPRO CULTA 3X
Manufacturer: Uriel Pharmacy, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 4d7af784-9f92-0dd5-e063-6394a90ab33b
SPL ID: 4d7af784-9f93-0dd5-e063-6394a90ab33b
Version: 1
Effective date: 2026-03-20
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:12:33

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Chamomilla Dec Cupro culta 3X	openfda.brand_name
generic name		CHAMOMILLA DEC CUPRO CULTA 3X	openfda.generic_name
manufacturer name		Uriel Pharmacy, Inc	openfda.manufacturer_name
ndc	package	48951-3284-3	openfda.package_ndc
ndc	product	48951-3284	openfda.product_ndc
ndc11	package	48951328403	derived:openfda.package_ndc
spl id		4d7af784-9f93-0dd5-e063-6394a90ab33b	id
spl set id		4d7af784-9f92-0dd5-e063-6394a90ab33b	set_id
unii		G0R4UBI2ZZ	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.