Label: ARNISPORT- arnica montana, hypericum perforatum, ruta graveolens flowering top, ledum palustre twig, bellis perennis, calcium fluoride, tribasic calcium phosphate, calcium sulfate anhydrous, ferrosoferric phosphate, potassium chloride, potassium phosphate, dibasic, potassium sulfate, magnesium phosphate, dibasic trihydrate, sodium chloride, sodium phosphate, dibasic, heptahydrate, sodium sulfate, and silicon dioxide tablet, soluble
- NDC Code(s): 54973-0232-1, 54973-0232-2, 54973-0232-3
- Packager: Hyland's
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated December 5, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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Drug Facts
Active ingredients
Arnica Montana 30X HPUS
Bellis Perennis 6X HPUS
Calcarea Fluorica 6X HPUS
Calcarea Phosphorica 3X HPUS
Calcarea Sulphurica 3X HPUS
Ferrum Phosphoricum 3X HPUS
Hypericum Perfoliatum 6X HPUS
Kali Muriaticum 3X HPUS
Kali Phosphoricum 3X HPUS
Kali Sulphuricum 3X HPUS
Ledum Palustre 6X HPUS
Magnesia Phosphorica 3X HPUS
Natrum Muriaticum 6X HPUS
Natrum Phosphoricum 3X HPUS
Natrum Sulphuricum 3X HPUS
Ruta Graveolens 6X HPUS
Silicea 6X HPUS
"HPUS" indicates that the active ingredients are in the official Homeopathic
Pharmacopoeia of the United States.
- Uses
- Warnings
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Directions
■ Use as directed.
Adults and children
12 years and overAt onset of symptoms, dissolve 2–3 tablets under tongue every 4 hours
as needed. If the initial dosage is not providing immediate relief, dissolve
2–3 tablets under tongue every 15 minutes until relieved, up to 6 doses.Children 6 years
to under 12 yearsAt onset of symptoms, dissolve 1–2 tablets under tongue every 4 hours
as needed. If the initial dosage is not providing immediate relief, dissolve
1 tablet under tongue every 15 minutes until relieved, up to 6 doses. - Inactive ingredients
- Questions?
- *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
- DO NOT USE IF TAMPER-EVIDENT SEAL IS BROKEN OR MISSING.
- PRINCIPAL DISPLAY PANEL - 50 Tablet Bottle Carton
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INGREDIENTS AND APPEARANCE
ARNISPORT
arnica montana, hypericum perforatum, ruta graveolens flowering top, ledum palustre twig, bellis perennis, calcium fluoride, tribasic calcium phosphate, calcium sulfate anhydrous, ferrosoferric phosphate, potassium chloride, potassium phosphate, dibasic, potassium sulfate, magnesium phosphate, dibasic trihydrate, sodium chloride, sodium phosphate, dibasic, heptahydrate, sodium sulfate, and silicon dioxide tablet, solubleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-0232 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM 6 [hp_X] RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP 6 [hp_X] LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P) LEDUM PALUSTRE TWIG 6 [hp_X] BELLIS PERENNIS (UNII: 2HU33I03UY) (BELLIS PERENNIS - UNII:2HU33I03UY) BELLIS PERENNIS 6 [hp_X] CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE 6 [hp_X] TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (PHOSPHATE ION - UNII:NK08V8K8HR) TRIBASIC CALCIUM PHOSPHATE 3 [hp_X] CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFATE ANHYDROUS 3 [hp_X] FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7) (FERRUM PHOSPHORICUM - UNII:91GQH8I5F7) FERRUM PHOSPHORICUM 3 [hp_X] POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 3 [hp_X] POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (POTASSIUM CATION - UNII:295O53K152, PHOSPHATE ION - UNII:NK08V8K8HR) POTASSIUM PHOSPHATE, DIBASIC 3 [hp_X] POTASSIUM SULFATE (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM SULFATE 3 [hp_X] MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 3 [hp_X] SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 6 [hp_X] SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B) (SODIUM CATION - UNII:LYR4M0NH37, PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 3 [hp_X] SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM SULFATE 3 [hp_X] SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 6 [hp_X] ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 30 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) ACACIA (UNII: 5C5403N26O) Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54973-0232-1 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/28/2000 2 NDC:54973-0232-2 4 in 1 POUCH; Type 0: Not a Combination Product 04/28/2000 3 NDC:54973-0232-3 4 in 1 CARTON 04/28/2000 3 4 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/28/2000 Labeler - Hyland's (028570695) Establishment Name Address ID/FEI Business Operations Standard Homeopathic Company 008316655 manufacture(54973-0232) , pack(54973-0232) , label(54973-0232) Establishment Name Address ID/FEI Business Operations Standard Homeopathic Company 080253323 manufacture(54973-0232) , pack(54973-0232) , label(54973-0232)