Oxalis 20% 1 [hp_X]/g
Oxalis 20% · OINTMENT · Uriel Pharmcy, Inc
Oxalis 20% is a ointment containing oxalis 20% at 1 [hp_X]/g, taken topical. Manufactured by Uriel Pharmcy, Inc.
Key Facts
- Brand Name
- Oxalis 20%
- Generic Name
- Oxalis 20%
- NDC Code (Product)
48951-7221- Manufacturer
- Uriel Pharmcy, Inc
- Strength
- 1 [hp_X]/g
- Dosage Form
- OINTMENT
- Route
- TOPICAL
- Marketing Status
- 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 Oxalis 20% used for?
Oxalis 20% contains Oxalis 20%. It is a ointment taken topical. Consult your doctor for specific uses.
Is Oxalis 20% a controlled substance?
Oxalis 20% is not classified as a controlled substance by the DEA.
What is the generic name for Oxalis 20%?
The generic name for Oxalis 20% is Oxalis 20%. There are no other listed brand versions of Oxalis 20%.
What is the NDC code for Oxalis 20% 1 [hp_X]/g?
The NDC (National Drug Code) for Oxalis 20% 1 [hp_X]/g is 48951-7221, listed by Uriel Pharmcy, Inc.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)