Acidum Oxalicum
- Product NDC
- 37662-2521
- 11-digit product format
- 376622521
- Labeler code
- 37662
- Product ID
- 37662-2521_f323df0f-a3ff-6230-e053-2995a90a6252
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acidum Oxalicum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Hahnemann Laboratories, INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2023-01-25
- Substance
- OXALIC ACID DIHYDRATE
- Active strength
- 1 [hp_M]/1
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 37662-2521-1 | 37662252101 | 200 PELLET in 1 VIAL, GLASS (37662-2521-1) | 200 pellet | 2023-01-25 | No | No | Historical |
| 37662-2521-2 | 37662252102 | 500 PELLET in 1 VIAL, GLASS (37662-2521-2) | 500 pellet | 2023-01-25 | No | No | Historical |
| 37662-2521-3 | 37662252103 | 3000 PELLET in 1 BOTTLE, GLASS (37662-2521-3) | 3000 pellet | 2023-01-25 | No | No | Historical |
| 37662-2521-4 | 37662252104 | 10000 PELLET in 1 BOTTLE, GLASS (37662-2521-4) | 10000 pellet | 2023-01-25 | No | No | Historical |