| NDC | 66096-177-06 |
| Set ID | 5deb690b-9471-4093-876d-8b2342bbedce |
| Category | HUMAN OTC DRUG LABEL |
| Packager | OHM PHARMA INC. |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number |
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ACTIVE INGREDIENT
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
- WARNINGS
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DOSAGE & ADMINISTRATION
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
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
OHM SPASTIC TERRAIN
aconitum napellus, arnica montana, belladonna, berberis vulgaris, bryonia alba, clematis erecta, colocynthis, cuprum aceticum, hypericum perforatum, symphytum officinale, veratum album. liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66096-177 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS 6 [hp_X] in 2.2 mL ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 5 [hp_X] in 2.2 mL ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 5 [hp_X] in 2.2 mL BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 4 [hp_X] in 2.2 mL BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 4 [hp_X] in 2.2 mL CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (CLEMATIS RECTA FLOWERING TOP - UNII:396421SP9F) CLEMATIS RECTA FLOWERING TOP 4 [hp_X] in 2.2 mL CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (CITRULLUS COLOCYNTHIS FRUIT PULP - UNII:23H32AOH17) CITRULLUS COLOCYNTHIS FRUIT PULP 4 [hp_X] in 2.2 mL CUPRIC ACETATE (UNII: 39M11XPH03) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC CATION 5 [hp_X] in 2.2 mL HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM 5 [hp_X] in 2.2 mL COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT 7 [hp_X] in 2.2 mL VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z) VERATRUM ALBUM ROOT 4 [hp_X] in 2.2 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66096-177-06 12 in 1 BOX 01/06/2017 1 2.2 mL in 1 AMPULE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/25/2011 Labeler - OHM PHARMA INC. (030572478) Registrant - OHM PHARMA INC. (030572478) Establishment Name Address ID/FEI Business Operations OHM PHARMA INC. 030572478 manufacture(66096-177)
