Oxalis e pl. tota 3
- Product NDC
- 48951-7109
- 11-digit product format
- 489517109
- Labeler code
- 48951
- Product ID
- 48951-7109_55de705b-a0a7-5519-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxalis e pl. tota 3
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- OXALIS ACETOSELLA LEAF
- Active strength
- 3 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-7109-1 | Oxalis e pl. tota 3 | 1 mL in 1 AMPULE | LIQUID | 1 | | 2 |
| 48951-7109-1 | Oxalis e pl. tota 3 | 10 in 1 BOX | LIQUID | 10 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-7109 | OXALIS E PL. TOTA 3 LIQUID [URIEL PHARMACY INC.] | 2 | Legacy NDC, 2 package rows | 20180529_448b0873-67f2-4e46-9f79-5f8f26bf7a39.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-7109-1 | 48951710901 | 10 AMPULE in 1 BOX (48951-7109-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |