FDA.reportPublic FDA data

OHM CIRCULATORY TERRAIN

Manufacturer
OHM PHARMA INC.
Effective date
2021-01-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:57:18

Label at a glance#

ProductOHM CIRCULATORY TERRAIN
Active ingredientBARIUM IODIDE, SELENICEREUS GRANDIFLORUS STEM, ACTIVATED CHARCOAL, HAWTHORN LEAF WITH FLOWER, TUBOCURARINE CHLORIDE, POTASSIUM CARBONATE, KALMIA LATIFOLIA LEAF, MELILOTUS OFFICINALIS TOP, NAJA NAJA VENOM, CLAVICEPS PURPUREA SCLEROTIUM, SOLANUM NIGRUM TOP, SPIGELIA ANTHELMIA
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*): Equal amounts of:  Baryta Iodata 12X, Cactus Grandiflorus 6X, Carbo Vegetabilis 12X, Crataegus Oxyacantha 6X, Curare 12X, Kali Carbonicum 7X, Kalmia Latifolia 6X, Melilotus Officinale 6X, Naja Tripudians 12X, Secale Cornutum 12X, Solanum Nigrum 12X, Spigelia Anthelmia 12X.

OTC - ACTIVE INGREDIENT SECTION

*The letters "HPUS" indicate the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.

INDICATIONS & USAGE SECTION

USES: Temporarily relieves cardio - circulatory ailments.**

INDICATIONS & USAGE SECTION

**This statement has not been evaluated by the FDA.
It is based on documented Homeopathic Materia Medica.

WARNINGS SECTION

WARNINGS:

IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. If symptoms worsen or persist for more than 5 days, discontinue use and contact a health care professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: To open ampoule snap top up and away from you. Using pipette place entire content under the tongue, hold it for 30 seconds and swallow.

POSOLOGY: Adults and children over 12 years: In acute conditions: 1 ampoule every 12 hours. In chronic conditions: 1 ampoule one to four times per week, or as directed by a health professional.

Children under 12 years use 1/2 the adult dose.

Discard unused solution. Solution does not contain any preservatives.

Not for injection.

OTHER SAFETY INFORMATION

OTHER INFORMATION: Store at controlled room temperature. Tamper evident seal. Do not use if box seal is missing or broken.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Isotonic sodium chloride solution.

OTC - QUESTIONS SECTION

Mfg. By: OHM PHARMA, INC. / Mineral Wells, TX 76067

Made in USA

www.ohmpharma.com

OTC - PURPOSE SECTION

Cardio - circulatory ailments relief

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 66096-179-06

OHM CIRCULATORY TERRAIN

HOMEOPATHIC MEDICINE

Pharmaceutical Grade. Professional use only.

CONTENTS: 12 oral ampoules of 2.2 ml each.

Terrain Label EnglishTerrain Label English

Terrain Label SpanishTerrain Label Spanish

Ampoule LabelAmpoule Label

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Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66096-17966096-179-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XIACT
BARIUM IODIDEWKC4T7680AACTIB
SELENICEREUS GRANDIFLORUS STEM7114SV0MYKACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
HAWTHORN LEAF WITH FLOWER6OM09RPY36ACTIB
TUBOCURARINE CHLORIDE900961Z8VRACTIB
POTASSIUM CARBONATEBQN1B9B9HAACTIB
KALMIA LATIFOLIA LEAF79N6542N18ACTIB
MELILOTUS OFFICINALIS TOPGM6P02J2DXACTIB
NAJA NAJA VENOMZZ4AG7L7VMACTIB
CLAVICEPS PURPUREA SCLEROTIUM01G9XEA93NACTIB
SOLANUM NIGRUM TOPO4G5C1G3W5ACTIB
SPIGELIA ANTHELMIAWYT05213GEACTIB

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
1abbd278-ba05-4208-a06a-7de553c7748caaca0517-a5fa-4496-a921-bc44cc7ec2b32021-03-25WarningsExact identifier
spl set id: aaca0517-a5fa-4496-a921-bc44cc7ec2b3

Reported adverse events (FAERS/openFDA)#

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