Quartz Oxalis Nicotiana
- Product NDC
- 48951-8111
- 11-digit product format
- 489518111
- Labeler code
- 48951
- Product ID
- 48951-8111_55ef60e5-bc07-313f-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Quartz Oxalis Nicotiana
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- SILVER; TOBACCO LEAF; OXALIS ACETOSELLA LEAF; SILICON DIOXIDE
- Active strength
- 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8111-1 | 48951811101 | 10 AMPULE in 1 BOX (48951-8111-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |