OHM Spastic Terrain
- Manufacturer
- OHM PHARMA INC.
- Effective date
- 2021-12-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:20:11
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENTS (HPUS*): Equal amounts of: Aconitum Napellus 6X, Arnica Montana 5X, Belladonna 5X, Berberis Vulgaris 4X, Bryonia Alba 4X, Clematis Erecta 4X, Colocynthis 4X, Cuprum Aceticum 5X, Hypericum Perforatum 5X, Symphytum Officinale 7X, Veratrum Album 4X.
**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 smooth muscle spasms.**
WARNINGS SECTION
WARNINGS: IF PREGNANT OR BREAST- FEEDING, ask a health professional before use. KEEP OUT OF THE REACH OF CHILDREN. 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.
**This statement has not been evaluated by the FDA. It is based on documented Homeopathic Materia Medica.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: Isotonic sodium chloride solution.
OTC - QUESTIONS SECTION
MFG. By: OHM PHARMA, INC. / Mineral Wells, TX 76067
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC: 66096-177-06
OHM SPASTIC TERRAIN
HOMEOPATHIC MEDICINE
Pharmaceutical Grade. Professional use only.
CONTENTS: 12 oral ampoules of 2.2 ml each
OTC - PURPOSE SECTION
Temporarily relieves smooth muscle spasms
Products#
Every source-derived product name is available through these pages.
- OHM Spastic Terrain
- Aconitum Napellus, Arnica Montana, Belladonna, Berberis Vulgaris, Bryonia Alba, Clematis Erecta, Colocynthis, Cuprum Aceticum, Hypericum Perforatum, Symphytum Officinale, Veratum Album.
- SODIUM CHLORIDE
- ACONITUM NAPELLUS
- ARNICA MONTANA
- ATROPA BELLADONNA
- BERBERIS VULGARIS ROOT BARK
- BRYONIA ALBA ROOT
- CLEMATIS RECTA FLOWERING TOP
- CITRULLUS COLOCYNTHIS FRUIT PULP
- CUPRIC ACETATE
- CUPRIC CATION
- HYPERICUM PERFORATUM
- COMFREY ROOT
- VERATRUM ALBUM ROOT
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 66096-177 | 66096-177-06 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| ACONITUM NAPELLUS | U0NQ8555JD | ACTIB |
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| ATROPA BELLADONNA | WQZ3G9PF0H | ACTIB |
| BERBERIS VULGARIS ROOT BARK | 1TH8Q20J0U | ACTIB |
| BRYONIA ALBA ROOT | T7J046YI2B | ACTIB |
| CLEMATIS RECTA FLOWERING TOP | 396421SP9F | ACTIB |
| CITRULLUS COLOCYNTHIS FRUIT PULP | 23H32AOH17 | ACTIB |
| CUPRIC ACETATE | 39M11XPH03 | ACTIM |
| HYPERICUM PERFORATUM | XK4IUX8MNB | ACTIB |
| COMFREY ROOT | M9VVZ08EKQ | ACTIB |
| VERATRUM ALBUM ROOT | QNS6W5US1Z | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 537bbd83-a864-43ea-b581-9e379b27d4c9 | 5deb690b-9471-4093-876d-8b2342bbedce | 2022-01-04 | Warnings | 5deb690b-9471-4093-876d-8b2342bbedce |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
