Ferrum Quartz
- Product NDC
- 48951-4062
- Requested package NDC
- 48951-4062-1
- 11-digit product format
- 489514062
- Labeler code
- 48951
- Product ID
- 48951-4062_6c7dcc74-a254-27b8-e053-2991aa0a9813
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ferrum Quartz
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- SANGUINARIA CANADENSIS ROOT; SULFUR; IRON; SILICON DIOXIDE
- Active strength
- 6 [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
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 package | package | 48951-4062 | 48951-4062-1 | I | Inactivated by FDA | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 910c1bd7-67d1-44c7-ad4f-9445f827edcc | Product name | 1 | 20230808 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-4062-1 | Ferrum Quartz | 1 mL in 1 AMPULE | LIQUID | 1 | 4 | |
| 48951-4062-1 | Ferrum Quartz | 10 in 1 BOX | LIQUID | 10 | 4 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| COLLOIDAL SILICON DIOXIDE | ACTIVE INGREDIENT | ETJ7Z6XBU4 | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| IRON | ACTIVE INGREDIENT | E1UOL152H7 | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| SANGUINARIA CANADENSIS ROOT | ACTIVE INGREDIENT | N9288CD508 | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| SULFUR | ACTIVE INGREDIENT | 70FD1KFU70 | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | ACTIVE MOIETY | ETJ7Z6XBU4 | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| IRON | ACTIVE MOIETY | E1UOL152H7 | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| SANGUINARIA CANADENSIS ROOT | ACTIVE MOIETY | N9288CD508 | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| SULFUR | ACTIVE MOIETY | 70FD1KFU70 | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-4062 | FERRUM QUARTZ LIQUID [URIEL PHARMACY INC.] | 4 | Legacy NDC, 2 package rows | 20241213_63c4a943-5450-4418-b18b-59461501c0bc.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 48951-4062-1 | 48951406201 | 10 AMPULE in 1 BOX (48951-4062-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |