Drosera Rotundifolia Kit Refill

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: Drosera Rotundifolia Kit Refill
Generic name: DROSERA ROTUNDIFOLIA
Manufacturer: Washington Homeopathic Products
Product type: HUMAN OTC DRUG
SPL set ID: deaaf6b3-0cc2-4813-e053-2995a90ac5d6
SPL ID: 2cc7e3f6-7987-ac73-e063-6294a90a2bc6
Version: 4
Effective date: 2025-01-28
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:36:59

Harmonized routes table
Harmonized routes
ORAL

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		Drosera Rotundifolia Kit Refill	openfda.brand_name
generic name		DROSERA ROTUNDIFOLIA	openfda.generic_name
manufacturer name		Washington Homeopathic Products	openfda.manufacturer_name
ndc	package	71919-761-01	openfda.package_ndc
ndc	product	71919-761	openfda.product_ndc
ndc11	package	71919076101	derived:openfda.package_ndc
spl id		2cc7e3f6-7987-ac73-e063-6294a90a2bc6	id
spl set id		deaaf6b3-0cc2-4813-e053-2995a90ac5d6	set_id
unii		QR44N9XPJQ	openfda.unii

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

Warnings sections page 1 of 1 · 1 matching rows.

STOP USE AND ASK DOCTOR If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

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