Bismuth Magnesite comp.
- Product NDC
- 48951-8307
- 11-digit product format
- 489518307
- Labeler code
- 48951
- Product ID
- 48951-8307_6a85e3c9-7a54-0672-e053-2a91aa0a680a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth Magnesite comp.
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-01-09
- Marketing end
- 0000-00-00
- Substance
- BISMUTH; ANTIMONY TRISULFIDE; SAFFRON; CORALLIUM RUBRUM EXOSKELETON; MAGNESITE; POTASSIUM ACETATE
- Active strength
- 3 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [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 |
|---|
| 48951-8307-4 | Bismuth Magnesite comp. | 50 g in 1 BOTTLE, GLASS | POWDER | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8307 | BISMUTH MAGNESITE COMP. POWDER [URIEL PHARMACY INC.] | 2 | Legacy NDC, 1 package rows | 20180503_3d0935dc-cacb-73ec-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8307-4 | 48951830704 | 50 g in 1 BOTTLE, GLASS (48951-8307-4) | 50 g | 2009-01-09 | 0000-00-00 | No | No | Current |