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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| U015TT5I8H | BISMUTH | 7440-69-9 | BISMUTH |
| F79059A38U | ANTIMONY TRISULFIDE | 1345-04-6 | ANTIMONY TRISULFIDE |
| E849G4X5YJ | SAFFRON | | SAFFRON |
| 2CA71K0DLE | CORALLIUM RUBRUM EXOSKELETON | | CORALLIUM RUBRUM EXOSKELETON |
| 0IHC698356 | MAGNESITE | 546-93-0 | MAGNESITE |
| M911911U02 | POTASSIUM ACETATE | 127-08-2 | POTASSIUM ACETATE |
Packages
| 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 |