44911-0659 : Spinapar Oral Liquid
| NDC: | 44911-0659 |
| Labeler: | Energique, Inc. |
| Product Type: | Human OTC Drug |
| Drug Name: | Spinapar |
| Dosage Form: | Oral Liquid |
| Rev. Date: |
NDC Package Codes:
- 44911-0659-1: 30 ML IN 1 BOTTLE, DROPPER (44911‑0659‑1)
Active Ingredients:
- Amanita Muscaria Fruiting Body
- Arnica Montana Whole
- Bambusa Bambos Leaf
- Bambusa Bambos Sap
- Bellis Perennis Whole
- Bryonia Alba Root
- Calcium Fluoride
- Harpagophytum Procumbens Root
- Horse Chestnut
- Hypericum Perforatum Whole
- Phytolacca Americana Root
- Ruta Graveolens Flowering Top
- Silver
- Sulfur
- Sus Scrofa Cartilage
- Sus Scrofa Intervertebral Disc
- Tellurium
- Toxicodendron Pubescens Leaf
Dosage Strength:
- 12 [hp_X]/mL
- 12 [hp_X]/mL
- 12 [hp_X]/mL
- 12 [hp_X]/mL
- 12 [hp_X]/mL
- 12 [hp_X]/mL
- 12 [hp_X]/mL
- 4 [hp_X]/mL
- 4 [hp_X]/mL
- 12 [hp_X]/mL
- 4 [hp_X]/mL
- 4 [hp_X]/mL
- 12 [hp_X]/mL
- 12 [hp_X]/mL
- 6 [hp_X]/mL
- 6 [hp_X]/mL
- 12 [hp_X]/mL
- 12 [hp_X]/mL
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.
