FDA.reportPublic FDA data

Lymphoplus

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2017-04-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:16:59

Label at a glance#

ProductLymphoplus
Active ingredientTRIFOLIUM PRATENSE FLOWER, SUS SCROFA LYMPH, SUS SCROFA SPLEEN, CONIUM MACULATUM FLOWERING TOP, ECHINACEA ANGUSTIFOLIA, LYCOPODIUM CLAVATUM SPORE, MYRRH, PHYTOLACCA AMERICANA ROOT, SELENIUM, SILICON DIOXIDE
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Trifolium Pratense 3X, Lymph Node (Suis) 8X, Spleen (Suis) 8X, Conium Maculatum 12X, Echinacea (Angustifolia) 12X, Lycopodium Clavatum 12X, Myrrha 12X, ,Phytolacca Decandra 12X, Selenium Metallicum 12X, Silicea 12X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of symptoms related to impaired function of the lymphatic system including fever, vertigo, earache, cough and infection.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms related to impaired function of the lymphatic system including fever, vertigo, earache, cough and infection.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070      www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0827-1

HOMEOPATHIC

LYMPHOPLUS

1 FL OZ (30 ml)

LymphoplusLymphoplus

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-082743742-0827-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRIFOLIUM PRATENSE FLOWER4JS0838828ACTIB
SUS SCROFA LYMPH33A7VYU29LACTIB
SUS SCROFA SPLEEN92AMN5J79YACTIB
CONIUM MACULATUM FLOWERING TOPQ28R5GF371ACTIB
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
MYRRHJC71GJ1F3LACTIB
PHYTOLACCA AMERICANA ROOT11E6VI8VEGACTIB
SELENIUMH6241UJ22BACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
dc427f6b-9059-476d-81d5-3e6c88e84ac4171e3f05-befd-4050-a417-9ff33052c9c82017-04-05WarningsExact identifier
spl id: dc427f6b-9059-476d-81d5-3e6c88e84ac4
spl set id: 171e3f05-befd-4050-a417-9ff33052c9c8

Reported adverse events (FAERS/openFDA)#

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