Cuprum Quartz (Red)
- Product NDC
- 48951-3152
- Requested package NDC
- 48951-3152-5
- 11-digit product format
- 489513152
- Labeler code
- 48951
- Product ID
- 48951-3152_57d39a95-de68-83c0-e053-2991aa0a6a4c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cuprum Quartz (Red)
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- SILICON DIOXIDE; CUPRIC OXIDE
- Active strength
- 1 [hp_X]/g; [hp_X]/g
- 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 | 48951-3152 | 48951-3152-5 | I | Inactivated by FDA | 2026-08-07 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-3152-5 | Cuprum Quartz (Red) | 60 g in 1 TUBE | OINTMENT | 60 | 2 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| COLLOIDAL SILICON DIOXIDE | ACTIVE INGREDIENT | ETJ7Z6XBU4 | CUPRUM QUARTZ (RED) OINTMENT [URIEL PHARMACY INC.] | 1 | |
| CUPRIC OXIDE | ACTIVE INGREDIENT | V1XJQ704R4 | CUPRUM QUARTZ (RED) OINTMENT [URIEL PHARMACY INC.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | ACTIVE MOIETY | ETJ7Z6XBU4 | CUPRUM QUARTZ (RED) OINTMENT [URIEL PHARMACY INC.] | 1 | |
| CUPRIC CATION | ACTIVE MOIETY | 8CBV67279L | CUPRUM QUARTZ (RED) OINTMENT [URIEL PHARMACY INC.] | 1 | |
| MINERAL OIL | INACTIVE INGREDIENT | T5L8T28FGP | CUPRUM QUARTZ (RED) OINTMENT [URIEL PHARMACY INC.] | 1 | |
| PETROLATUM | INACTIVE INGREDIENT | 4T6H12BN9U | CUPRUM QUARTZ (RED) OINTMENT [URIEL PHARMACY INC.] | 1 | |
| ROSEMARY OIL | INACTIVE INGREDIENT | 8LGU7VM393 | CUPRUM QUARTZ (RED) OINTMENT [URIEL PHARMACY INC.] | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-3152 | CUPRUM QUARTZ (RED) OINTMENT [URIEL PHARMACY INC.] | 2 | Legacy NDC, 1 package rows | 20181212_cb6aabfb-bf65-4cfa-a1e5-e79fd5931398.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 48951-3152-5 | 48951315205 | 60 g in 1 TUBE (48951-3152-5) | 60 g | 2009-09-01 | 0000-00-00 | No | No | Current |