Melange combination
- Product NDC
- 62106-1235
- 11-digit product format
- 621061235
- Labeler code
- 62106
- Product ID
- 62106-1235_c71e791a-cfbb-6f52-e053-2995a90af4d4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcarea sulphurica, Calcium phosphoricum, Kali muriaticum, Kalium phosphoricum, Kali sulphuricum, Magnesia phosphorica, Natrum muriaticum, Natrum phosphoricum, Natrium sulfuricum, Calcarea fluorica, Ferrum phosphoricum, Silicea
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Seroyal USA
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-12-12
- Substance
- CALCIUM FLUORIDE; CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS; CALCIUM SULFATE ANHYDROUS; FERROSOFERRIC PHOSPHATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM SULFATE; SILICON DIOXIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATE
- Active strength
- 12; 6; 6; 12; 6; 6; 6; 6; 12; 6; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Melange combination
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS | 12 [hp_X]/1 |
| POTASSIUM CHLORIDE | 6 [hp_X]/1 |
| POTASSIUM PHOSPHATE, DIBASIC | 6 [hp_X]/1 |
| CALCIUM SULFATE ANHYDROUS | 12 [hp_X]/1 |
| SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE | 6 [hp_X]/1 |
| SILICON DIOXIDE | 6 [hp_X]/1 |
| POTASSIUM SULFATE | 6 [hp_X]/1 |
| MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE | 6 [hp_X]/1 |
| SODIUM CHLORIDE | 12 [hp_X]/1 |
| SODIUM SULFATE | 6 [hp_X]/1 |
| CALCIUM FLUORIDE | 6 [hp_X]/1 |
| FERROSOFERRIC PHOSPHATE | 6 [hp_X]/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| L11K75P92J | Internal UNII lookup |
| 660YQ98I10 | Internal UNII lookup |
| CI71S98N1Z | Internal UNII lookup |
| E934B3V59H | Internal UNII lookup |
| 70WT22SF4B | Internal UNII lookup |
| ETJ7Z6XBU4 | Internal UNII lookup |
| 1K573LC5TV | Internal UNII lookup |
| HF539G9L3Q | Internal UNII lookup |
| 451W47IQ8X | Internal UNII lookup |
| 0YPR65R21J | Internal UNII lookup |
| O3B55K4YKI | Internal UNII lookup |
| 91GQH8I5F7 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 0a071fbf-0075-4479-e054-00144ff8d46c | Available on FDA.report |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62106-1235-2 | Melange combination | 100 in 1 BOTTLE, GLASS | TABLET | 100 | 9 | |
| 62106-1235-2 | Melange combination | 1 in 1 BOX | TABLET | 1 | 9 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62106-1235 | MELANGE COMBINATION (CALCAREA SULPHURICA, CALCIUM PHOSPHORICUM, KALI MURIATICUM, KALIUM PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRIUM SULFURICUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, SILICEA) TABLET [SEROYAL USA] | 9 | Current NDC, Legacy NDC, 2 package rows | 20210715_0a071fbf-0075-4479-e054-00144ff8d46c.zip |
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 |
|---|---|---|---|---|---|---|
| Melange combination | CALCAREA SULPHURICA, CALCIUM PHOSPHORICUM, KALI MURIATICUM, KALIUM PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRIUM SULFURICUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, SILICEA | Seroyal USA | 0a071fbf-0075-4479-e054-00144ff8d46c | 2021-07-14 | Warnings | 62106-1235 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 62106-1235-2 | 62106123502 | 1 BOTTLE, GLASS in 1 BOX (62106-1235-2) / 100 TABLET in 1 BOTTLE, GLASS | 2014-12-16 | 0000-00-00 | No | No | Current |