Bambusa Argentum
- Product NDC
- 48951-2138
- 11-digit product format
- 489512138
- Labeler code
- 48951
- Product ID
- 48951-2138_b70fd0b9-22bb-a955-e053-2a95a90ab672
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bambusa Argentum
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- BAMBUSA VULGARIS WHOLE; STACHYS OFFICINALIS; ROSMARINUS OFFICINALIS FLOWERING TOP; GOLD; BOS TAURUS INTERVERTEBRAL DISC; COPPER; SILICON DIOXIDE; SILVER; ARNICA MONTANA
- Active strength
- 8 [hp_X]/g; [hp_X]/g; [hp_X]/g; [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
- 2021-12-31
- 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 |
|---|
| 48951-2138-5 | Bambusa Argentum | 60 g in 1 TUBE | GEL | 60 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-2138 | BAMBUSA ARGENTUM GEL [URIEL PHARMACY INC.] | 4 | Legacy NDC, 1 package rows | 20201224_2e11a55c-20b4-466d-a313-2f008f53b5c2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-2138-5 | 48951213805 | 60 g in 1 TUBE (48951-2138-5) | 60 g | 2009-09-01 | 0000-00-00 | No | No | Current |