Oxalis 5
- Product NDC
- 48951-7227
- 11-digit product format
- 489517227
- Labeler code
- 48951
- Product ID
- 48951-7227_5d1ac5ee-cbcb-5616-e063-6394a90a3439
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxalis 5
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- OXALIS ACETOSELLA LEAF
- Active strength
- 5 [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Oxalis 5
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXALIS ACETOSELLA LEAF | 5 [hp_X]/g |
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-7227-5 | 48951722705 | 60 g in 1 TUBE (48951-7227-5) | 60 g | 2009-09-01 | No | No | Current |