HBP

Manufacturer
Newton Laboratories, Inc.
Effective date
2019-12-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:49:17

Label at a glance#

ProductHBP
Active ingredientMICRURUS CORALLINUS VENOM, VISCUM ALBUM FRUITING TOP, RUTA GRAVEOLENS FLOWERING TOP, VIPERA BERUS VENOM, EPINEPHRINE, ARSENIC TRIOXIDE, GOLD, BARIUM CARBONATE, BRYONIA ALBA ROOT, SELENICEREUS GRANDIFLORUS STEM, CHELIDONIUM MAJUS, CINCHONA OFFICINALIS BARK, CROTALUS HORRIDUS HORRIDUS VENOM, DIGITALIS, NITROGLYCERIN, POTASSIUM CARBONATE, POTASSIUM IODIDE, LACHESIS MUTA VENOM, NAJA NAJA VENOM, STRYCHNOS NUX-VOMICA SEED, VERATRUM ALBUM ROOT, VALERIAN
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Formulated for associated symptoms such as headache, ear ringing, anxiety, sweating, pallor and nausea.

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 drops by mouth one to four times daily or as directed by a health professional.

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Ruta graveolens 6x, Valeriana officinalis 6x, Adrenalinum 15x, Arsenicum iodatum 15x, Aurum metallicum 15x, Baryta carbonica 15x, Bryonia 15x, Cactus grandiflorus 15x, Chelidonium majus 15x, Cinchona officinalis 15x, Crotalus horridus 15x, Digitalis purpurea 15x, Glonoinum 15x, Kali carbonicum 15x, Kali iodatum 15x, Lachesis mutus 15x, Naja tripudians 15x, Nux vomica 15x, Veratrum album 15x, Vipera berus 15x, Viscum album 15x, Elaps corallinus 30x.

OTC - PURPOSE SECTION

Formulated for associated symptoms such as headache, ear ringing, anxiety, sweating, pallor and nausea.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net - Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 Conyers, GA 30013

WARNINGS SECTION

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-477055714-4770-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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
b5945530-8c2f-6e63-e053-2a95a90ae98f9a15d516-c84c-9204-e053-2995a90ac13f2020-12-03WarningsExact identifier
spl set id: 9a15d516-c84c-9204-e053-2995a90ac13f

Reported adverse events (FAERS/openFDA)#

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