Silica
- Product NDC
- 48951-8317
- 11-digit product format
- 489518317
- Labeler code
- 48951
- Product ID
- 48951-8317_551153e9-cc50-5cb8-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Silica
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- EQUISETUM ARVENSE TOP; WHITE OAK BARK; MAMMAL LIVER
- Active strength
- 5 [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-8317-7 | Silica | 1 in 1 BOTTLE, GLASS | POWDER | 1 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8317 | SILICA POWDER [URIEL PHARMACY INC] | 2 | Legacy NDC, 1 package rows | 20170724_32840bc0-2dfb-11df-8a39-0800200c9a66.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8317-7 | 48951831707 | 1 POWDER in 1 BOTTLE, GLASS (48951-8317-7) | 1 powder | 2009-09-01 | 0000-00-00 | No | No | Current |