Stibium 6X
- Product NDC
- 48951-8401
- 11-digit product format
- 489518401
- Labeler code
- 48951
- Product ID
- 48951-8401_2c286b32-d8b5-9c06-e063-6394a90a3fbc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Stibium 6X
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- ANTIMONY
- Active strength
- 6 [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Stibium 6X
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ANTIMONY | 6 [hp_X]/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9IT35J3UV3 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-8401-4 | Stibium 6X | 50 g in 1 BOTTLE, GLASS | POWDER | 50 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8401 | STIBIUM 6X POWDER [URIEL PHARMACY INC.] | 5 | Current NDC, 1 package rows | 20250121_0a1f3d5d-13d5-97b3-e063-6394a90aa250.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-8401-4 | 48951840104 | 50 g in 1 BOTTLE, GLASS (48951-8401-4) | 50 g | 2009-09-01 | No | No | Current |