Cuprum 0.4
- Product NDC
- 48951-3280
- 11-digit product format
- 489513280
- Labeler code
- 48951
- Product ID
- 48951-3280_2c8fc7ec-a8ff-7468-e063-6294a90ae355
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cuprum 0.4
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- COPPER
- Active strength
- 1 [hp_X]/g
- Pharmacologic classes
- Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cuprum 0.4
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| COPPER | 1 [hp_X]/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 789U1901C5 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-3280-2 | Cuprum 0.4 | 30 g in 1 TUBE | OINTMENT | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-3280 | CUPRUM 0.4 OINTMENT [URIEL PHARMACY, INC] | 1 | Current NDC, 1 package rows | 20250127_2c8fc7ec-a8fe-7468-e063-6294a90ae355.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-3280-2 | 48951328002 | 30 g in 1 TUBE (48951-3280-2) | 30 g | 2009-09-01 | No | No | Current |