Scorodite Prunus 8 [hp_X]/mL
Scorodite Prunus · LIQUID · Uriel Pharmacy Inc.
Scorodite Prunus is a liquid containing scorodite prunus at 8 [hp_X]/mL, taken oral. Manufactured by Uriel Pharmacy Inc..
Key Facts
- Brand Name
- Scorodite Prunus
- Generic Name
- Scorodite Prunus
- NDC Code (Product)
48951-8168- Manufacturer
- Uriel Pharmacy Inc.
- Strength
- 8 [hp_X]/mL
- Dosage Form
- LIQUID
- Route
- ORAL
- Marketing Status
- Drug Class
- Standardized Chemical Allergen [EPC]
- Marketing Start
- 09/01/2009
Recall History
No Recall HistoryFull Prescribing Information
Indications & Usage
Directions: FOR ORAL USE ONLY.
Dosage & Administration
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditons worsen or persist. If pregnant or nursing consult a doctor before use.
Frequently Asked Questions
What is Scorodite Prunus used for?
Scorodite Prunus contains Scorodite Prunus. It is a liquid taken oral. Consult your doctor for specific uses.
Is Scorodite Prunus a controlled substance?
Scorodite Prunus is not classified as a controlled substance by the DEA.
What is the generic name for Scorodite Prunus?
The generic name for Scorodite Prunus is Scorodite Prunus. There are no other listed brand versions of Scorodite Prunus.
What is the NDC code for Scorodite Prunus 8 [hp_X]/mL?
The NDC (National Drug Code) for Scorodite Prunus 8 [hp_X]/mL is 48951-8168, listed by Uriel Pharmacy Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)