Argentum Viscum
- Product NDC
- 48951-1313
- Requested package NDC
- 48951-1313-1
- 11-digit product format
- 489511313
- Labeler code
- 48951
- Product ID
- 48951-1313_7ef670a1-b87b-f187-e053-2a91aa0a9f9c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Argentum Viscum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- SILVER CHLORIDE; VISCUM ALBUM FRUITING TOP; BOS TAURUS EYE
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1313-1 | Argentum Viscum | 10 mL in 1 BOTTLE, DROPPER | LIQUID | 10 | | 2 |
| 48951-1313-1 | Argentum Viscum | 1 in 1 BAG | LIQUID | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1313 | ARGENTUM VISCUM LIQUID [URIEL PHARMACY INC.] | 2 | Legacy NDC, 2 package rows | 20240119_7ef670a1-b87a-f187-e053-2a91aa0a9f9c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1313-1 | 48951131301 | 1 BOTTLE, DROPPER in 1 BAG (48951-1313-1) > 10 mL in 1 BOTTLE, DROPPER | 2009-09-01 | 0000-00-00 | No | No | Current |