Lymph Drainage

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: Lymph Drainage
Generic name: BAPTISIA TINCTORIA, CITRUS LIMONUM, ECHINACEA (ANGUSTIFOLIA), LOBELIA INFLATA, PHYTOLACCA DECANDRA, PINUS SYLVESTRIS, TEUCRIUM SCORODONIA, THUJA OCCIDENTALIS, CAPSICUM ANNUUM, CUPRUM SULPHURICUM, KALI MURIATICUM, MANGANUM MURIATICUM, ARSENICUM IODATUM, CARPINUS BETULUS, FLOS, CENTAURIUM UMBELLATUM, FLOS, GALIUM APARINE, LARIX DECIDUA, FLOS, ROSA CANINA, SCROPHULARIA NODOSA, ZINCUM GLUCONICUM, ARANEA DIADEMA, CALCAREA CARBONICA, CARBO VEGETABILIS, CEANOTHUS AMERICANUS, LACHESIS MUTUS
Manufacturer: Carnivora Research International
Product type: HUMAN OTC DRUG
SPL set ID: 57be5edd-a45b-40e4-b095-fafbfd3dc703
SPL ID: d80c0297-d129-47b8-b526-9ac474c215d8
Version: 2
Effective date: 2026-04-20
Source export date: 2026-10-12
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:40:06

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 · 33 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Lymph Drainage	openfda.brand_name
generic name		BAPTISIA TINCTORIA, CITRUS LIMONUM, ECHINACEA (ANGUSTIFOLIA), LOBELIA INFLATA, PHYTOLACCA DECANDRA, PINUS SYLVESTRIS, TEUCRIUM SCORODONIA, THUJA OCCIDENTALIS, CAPSICUM ANNUUM, CUPRUM SULPHURICUM, KALI MURIATICUM, MANGANUM MURIATICUM, ARSENICUM IODATUM, CARPINUS BETULUS, FLOS, CENTAURIUM UMBELLATUM, FLOS, GALIUM APARINE, LARIX DECIDUA, FLOS, ROSA CANINA, SCROPHULARIA NODOSA, ZINCUM GLUCONICUM, ARANEA DIADEMA, CALCAREA CARBONICA, CARBO VEGETABILIS, CEANOTHUS AMERICANUS, LACHESIS MUTUS	openfda.generic_name
manufacturer name		Carnivora Research International	openfda.manufacturer_name
ndc	package	69134-0002-1	openfda.package_ndc
ndc	product	69134-0002	openfda.product_ndc
ndc11	package	69134000201	derived:openfda.package_ndc
spl id		d80c0297-d129-47b8-b526-9ac474c215d8	id
spl set id		57be5edd-a45b-40e4-b095-fafbfd3dc703	set_id
unii		2P3VWU3H10	openfda.unii
unii		00UK7646FG	openfda.unii
unii		9UMZ642257	openfda.unii
unii		11E6VI8VEG	openfda.unii
unii		LRX7AJ16DT	openfda.unii
unii		9PP1T3TC5U	openfda.unii
unii		5K1UO2888Y	openfda.unii
unii		3029988O2T	openfda.unii
unii		AGN709ANTJ	openfda.unii
unii		1NT28V9397	openfda.unii
unii		6T6CO7R3Z5	openfda.unii
unii		3TNW8D08V3	openfda.unii
unii		2E32821G6I	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		QQE170PANO	openfda.unii
unii		Q1RGP4UB73	openfda.unii
unii		QOI241B01F	openfda.unii
unii		660YQ98I10	openfda.unii
unii		B204P54Z1F	openfda.unii
unii		25B1Y14T8N	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		U6WSN5SQ1Z	openfda.unii
unii		LOK3I16O7G	openfda.unii
unii		Z4B6561488	openfda.unii
unii		7H443NUB2T	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: Do not use ■ if tamper evident seal around neck is broken or missing. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Sore throat warning if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Reported adverse events (FAERS/openFDA)#

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