OXALICUM ACIDUM
- Product NDC
- 0220-3838
- 11-digit product format
- 002203838
- Labeler code
- 0220
- Product ID
- 0220-3838_3a9d4e84-118f-0eca-e063-6294a90a73cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OXALIC ACID DIHYDRATE
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-01-01
- Substance
- OXALIC ACID DIHYDRATE
- Active strength
- 200 [kp_C]/200[kp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0K2L2IJ59O | OXALIC ACID DIHYDRATE | 6153-56-6 | OXALIC ACID DIHYDRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-3838-41 | 00220383841 | 200 [kp_C] in 1 TUBE (0220-3838-41) | 2025-01-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| OXALICUM ACIDUM 200CK | Boiron | Boiron, Inc. | 2025-07-23 | HUMAN OTC DRUG LABEL | 1 |