Cartilago Betula 6 [hp_X]/1
Cartilago Betula · PELLET · Uriel Pharmacy Inc.
Cartilago Betula is a pellet containing cartilago betula at 6 [hp_X]/1, taken oral. Manufactured by Uriel Pharmacy Inc..
Key Facts
- Brand Name
- Cartilago Betula
- Generic Name
- Cartilago Betula
- NDC Code (Product)
48951-3041- Manufacturer
- Uriel Pharmacy Inc.
- Strength
- 6 [hp_X]/1
- Dosage Form
- PELLET
- Route
- ORAL
- Marketing Status
- Drug Class
- Standardized Chemical Allergen [EPC]; Non-Standardized Food Allergenic Extract [EPC]
- Marketing Start
- 09/01/2009
Recall History
No Recall HistoryFull Prescribing Information
Indications & Usage
Directions: FOR TOPICAL USE ONLY.
Dosage & Administration
Apply to skin as needed. Under age 2: Consult a doctor.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.
Frequently Asked Questions
What is Cartilago Betula used for?
Cartilago Betula contains Cartilago Betula. It is a pellet taken oral. Consult your doctor for specific uses.
Is Cartilago Betula a controlled substance?
Cartilago Betula is not classified as a controlled substance by the DEA.
What is the generic name for Cartilago Betula?
The generic name for Cartilago Betula is Cartilago Betula. There are no other listed brand versions of Cartilago Betula.
What is the NDC code for Cartilago Betula 6 [hp_X]/1?
The NDC (National Drug Code) for Cartilago Betula 6 [hp_X]/1 is 48951-3041, listed by Uriel Pharmacy Inc..
Other Cartilago Betula Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)