Bryophyllum Quartz
- Product NDC
- 48951-2113
- 11-digit product format
- 489512113
- Labeler code
- 48951
- Product ID
- 48951-2113_6d853b54-f0f0-8d03-e053-2991aa0a30ac
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bryophyllum Quartz
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- KALANCHOE DAIGREMONTIANA LEAF; SILVER; OSTREA EDULIS SHELL; SILICON DIOXIDE
- Active strength
- 4 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 48951-2113 | I | Inactivated by FDA | 2026-10-05 | ||
| excluded package | package | 48951-2113 | 48951-2113-2 | I | Inactivated by FDA | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-2113-2 | Bryophyllum Quartz | 1350 in 1 BOTTLE, GLASS | PELLET | 1350 | 3 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| COLLOIDAL SILICON DIOXIDE | ACTIVE INGREDIENT | ETJ7Z6XBU4 | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 | |
| KALANCHOE DAIGREMONTIANA LEAF | ACTIVE INGREDIENT | L6X13JKL8O | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 | |
| OSTREA EDULIS SHELL | ACTIVE INGREDIENT | 49OY13BE7Z | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 | |
| SILVER | ACTIVE INGREDIENT | 3M4G523W1G | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | ACTIVE MOIETY | ETJ7Z6XBU4 | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 | |
| KALANCHOE DAIGREMONTIANA LEAF | ACTIVE MOIETY | L6X13JKL8O | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 | |
| OSTREA EDULIS SHELL | ACTIVE MOIETY | 49OY13BE7Z | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 | |
| SILVER | ACTIVE MOIETY | 3M4G523W1G | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-2113 | BRYOPHYLLUM QUARTZ PELLET [URIEL PHARMACY INC.] | 3 | Legacy NDC, 1 package rows | 20180601_b757a7a8-0ff5-4d64-9de3-bee32610fb17.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 48951-2113-2 | 48951211302 | 1350 PELLET in 1 BOTTLE, GLASS (48951-2113-2) | 1350 pellet | 2009-09-01 | 0000-00-00 | No | No | Current |