Formica Oxalis
- Product NDC
- 48951-4203
- Requested package NDC
- 48951-4203-3
- 11-digit product format
- 489514203
- Labeler code
- 48951
- Product ID
- 48951-4203_5d1997e3-80f7-7c9c-e063-6294a90a6df0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Formica Oxalis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- OXALIS ACETOSELLA LEAF; FORMICA RUFA
- Active strength
- 3; 5 [hp_X]/mL; [hp_X]/mL
- 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
- Formica Oxalis
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXALIS ACETOSELLA LEAF | 3 [hp_X]/mL |
| FORMICA RUFA | 5 [hp_X]/mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-4203-3 | 48951420303 | 60 mL in 1 BOTTLE, DROPPER (48951-4203-3) | 60 ml | 2009-09-01 | No | No | Current |