Bismuth Stibium
- Product NDC
- 48951-2132
- 11-digit product format
- 489512132
- Labeler code
- 48951
- Product ID
- 48951-2132_7cc55492-bebe-5445-e053-2a91aa0a3941
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth Stibium
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- GARLIC; CHELIDONIUM MAJUS; TURMERIC; THUJA OCCIDENTALIS WHOLE; BISMUTH; ANTIMONY
- Active strength
- 1 [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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-2132-5 | 48951213205 | 60 g in 1 TUBE (48951-2132-5) | 60 g | 2009-09-01 | 0000-00-00 | No | No | Current |