Herpes Simplex Plus

Manufacturer
Deseret Biologicals,Inc. | Apotheca Company
Effective date
2022-09-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:53:57

Label at a glance#

ProductHerpes Simplex Plus
Active ingredientGARLIC, CALENDULA OFFICINALIS FLOWERING TOP, SAMBUCUS NIGRA FLOWERING TOP, CLEMATIS RECTA FLOWERING TOP, SOLANUM DULCAMARA TOP, KEROSENE, SMILAX ORNATA ROOT, GRAPHITE, ARSENIC TRIOXIDE, CROTON TIGLIUM SEED, MERCURIC SULFIDE, SODIUM CHLORIDE, NITRIC ACID, TOXICODENDRON PUBESCENS LEAF, SEPIA OFFICINALIS JUICE, THUJA OCCIDENTALIS LEAFY TWIG
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

Allium Sativum 2X, Calendula Officinalis 2X, Sambucus Nigra 3X, Clematis Erecta 6X, Dulcamara 6X, Petroleum 6X, Sarsaparilla (Smilax Regelii) 6X, Graphites 8X, Arsenicum Album 12X, Croton Tiglium 12X, Mercurius Sulphuratus Ruber 12X, Natrum Muriaticum 12X, Nitricum Acidum 12X, Rhus Tox 12X, Sepia 12X, Thuja Occidentalis 12X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of symptoms of Herpes Simplex such as painful eruptions of lips, genitals, vesicular/blister of lips and genitals, tingling of lips, fatigue, irritability, fever, body aches and burning during urination.**

**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 physician or a 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 physician or a 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 of Herpes Simplex such as painful eruptions of lips, genitals, vesicular/blister of lips and genitals, tingling of lips, fatigue, irritability, fever, body aches and burning during urination.**

**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 43742-1047-1

HOMEOPATHIC

HERPES

SIMPLEX PLUS

1 FL OZ (30 ml)

Herpes Simplex PlusHerpes Simplex Plus

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-104743742-1047-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

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
046ce759-71e7-4b8e-a080-748f6b337d77119803cd-22be-4eea-8f65-d2f6cbadbf5b2022-09-12WarningsExact identifier
spl id: 046ce759-71e7-4b8e-a080-748f6b337d77
spl set id: 119803cd-22be-4eea-8f65-d2f6cbadbf5b

Reported adverse events (FAERS/openFDA)#

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