Oxalis 20%
- Product NDC
- 48951-7221
- 11-digit product format
- 489517221
- Labeler code
- 48951
- Product ID
- 48951-7221_3b52ff8d-4b88-d598-e063-6294a90aebd0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxalis 20%
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Uriel Pharmcy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- OXALIS STRICTA WHOLE
- Active strength
- 1 [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Oxalis 20%
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXALIS STRICTA WHOLE | 1 [hp_X]/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3STW243384 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-7221-5 | Oxalis 20% | 60 g in 1 TUBE | OINTMENT | 60 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-7221-5 | 48951722105 | 60 g in 1 TUBE (48951-7221-5) | 60 g | 2009-09-01 | No | No | Current |