Platinum Cichorium
- Product NDC
- 48951-8042
- 11-digit product format
- 489518042
- Labeler code
- 48951
- Product ID
- 48951-8042_55df46f4-c00f-2896-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Platinum Cichorium
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- CICHORIUM INTYBUS WHOLE; OXALIS ACETOSELLA LEAF; ROSMARINUS OFFICINALIS FLOWERING TOP; ACTIVATED CHARCOAL; SUS SCROFA PANCREAS; PLATINUM
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 1KE45XD28S | CICHORIUM INTYBUS WHOLE | | CICHORIUM INTYBUS WHOLE |
| U1W3U02EW0 | OXALIS ACETOSELLA LEAF | | OXALIS ACETOSELLA LEAF |
| 8JM482TI79 | ROSMARINUS OFFICINALIS FLOWERING TOP | | ROSMARINUS OFFICINALIS FLOWERING TOP |
| 2P3VWU3H10 | ACTIVATED CHARCOAL | 64365-11-3 | ACTIVATED CHARCOAL |
| 9Y3J3362RY | SUS SCROFA PANCREAS | | SUS SCROFA PANCREAS |
| 49DFR088MY | PLATINUM | 7440-06-4 | PLATINUM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8042-1 | 48951804201 | 10 AMPULE in 1 BOX (48951-8042-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Platinum Cichorium | Uriel Pharmacy Inc. | 2017-08-03 | HUMAN OTC DRUG LABEL | 2 |