Oxalis Belladonna
- Product NDC
- 48951-7108
- Requested package NDC
- 48951-7108-3
- 11-digit product format
- 489517108
- Labeler code
- 48951
- Product ID
- 48951-7108_6ad9a552-12c1-381e-e053-2991aa0a8b90
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxalis Belladonna
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- ATROPA BELLADONNA; MATRICARIA RECUTITA; GELSEMIUM SEMPERVIRENS ROOT; OXALIS ACETOSELLA LEAF; SANGUINARIA CANADENSIS ROOT
- Active strength
- 4 [hp_X]/mL; [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
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-7108-3 | Oxalis Belladonna | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-7108 | OXALIS BELLADONNA LIQUID [URIEL PHARMACY INC.] | 4 | Legacy NDC, 1 package rows | 20180427_ef43242e-7027-4495-aa84-f4a20496f593.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-7108-3 | 48951710803 | 60 mL in 1 BOTTLE, DROPPER (48951-7108-3) | 60 ml | 2009-09-01 | 0000-00-00 | No | No | Current |