NDC 48951-2161 – Berberis Oxalis
Berberis Vulgaris Root Bark 2 [hp_X]/mL; Oxalis Stricta Whole 3 [hp_X]/mL; Saw Palmetto 3 [hp_X]/mL; Urtica Urens 3 [hp_X]/mL; Viscum Album Fruiting Top 4… · Liquid · Oral
Product NDC48951-2161
Product details
- Brand name
- Berberis Oxalis
- Generic name
- Berberis Oxalis
- Labeler
- Uriel Pharmacy Inc.
- Dosage form
- Liquid
- Route
- Oral
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketed since
- September 1, 2009
- Listing expires
- December 31, 2027
- Pharmacologic class
- Calculi Dissolution Agent; Osmotic Laxative; Parenteral Iron Replacement; Phosphate Binder
Active ingredients
- Berberis Vulgaris Root Bark 2 [hp_X]/mL
- Oxalis Stricta Whole 3 [hp_X]/mL
- Saw Palmetto 3 [hp_X]/mL
- Urtica Urens 3 [hp_X]/mL
- Viscum Album Fruiting Top 4 [hp_X]/mL
- Magnesium Sulfate, Unspecified Form 6 [hp_X]/mL
- Bos Taurus Prostate Gland 8 [hp_X]/mL
- Penoxsulam 10 [hp_X]/mL
- Ferric Picrate 8 [hp_X]/mL
Uses, dosage, side effects and warnings for Berberis Oxalis →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 48951-2161-1 | 10 AMPULE in 1 BOX (48951-2161-1) / 1 mL in 1 AMPULE | Sep 1, 2009 |