Cuprum Quartz (Red)
- Product NDC
- 48951-3152
- 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| 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 table| 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 |