Amnion Oxalis comp.
- Product NDC
- 48951-1396
- 11-digit product format
- 489511396
- Labeler code
- 48951
- Product ID
- 48951-1396_2d7f3585-002c-854b-e063-6294a90ab9fa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Amnion Oxalis comp.
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- AMNIOTIC FLUID (BOVINE); KALANCHOE DAIGREMONTIANA LEAF; OXALIS STRICTA WHOLE
- Active strength
- 30; 3; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Matched term |
|---|
| P06X62O7E9 | AMNIOTIC FLUID (BOVINE) | AMNIOTIC FLUID (BOVINE) |
| L6X13JKL8O | KALANCHOE DAIGREMONTIANA LEAF | KALANCHOE DAIGREMONTIANA LEAF |
| 3STW243384 | OXALIS STRICTA WHOLE | OXALIS STRICTA WHOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-1396-3 | 48951139603 | 60 mL in 1 BOTTLE, DROPPER (48951-1396-3) | 60 ml | 2009-09-01 | No | No | Historical |