Koromiko 2X
- Product NDC
- 48951-6085
- Requested package NDC
- 48951-6085-3
- 11-digit product format
- 489516085
- Labeler code
- 48951
- Product ID
- 48951-6085_58b7ffcf-b913-377f-e063-6294a90adb7f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Koromiko 2X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- HEIMIA SALICIFOLIA LEAF
- Active strength
- 2 [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
- Koromiko 2X
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| HEIMIA SALICIFOLIA LEAF | 2 [hp_X]/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 0K96FZ8ZI2 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 58b7ffcf-b912-377f-e063-6294a90adb7f | Available on FDA.report |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Koromiko 2X | KOROMIKO 2X | Uriel Pharmacy, Inc | 58b7ffcf-b912-377f-e063-6294a90adb7f | 2026-08-10 | Warnings | 48951-6085-3 48951-6085 48951608503 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 48951-6085-3 | 48951608503 | 60 mL in 1 BOTTLE, DROPPER (48951-6085-3) | 60 ml | 2009-09-01 | No | No | Current |