Astragalus Formica
- Product NDC
- 48951-1174
- 11-digit product format
- 489511174
- Labeler code
- 48951
- Product ID
- 48951-1174_4bae0a05-ae26-cd5d-e063-6394a90ab841
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Astragalus Formica
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- ARNICA MONTANA; ASTRAGALUS PROPINQUUS ROOT; FORMICA RUFA; SILVER
- Active strength
- 3; 3; 6; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Astragalus Formica
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARNICA MONTANA | 3 [hp_X]/mL |
| ASTRAGALUS PROPINQUUS ROOT | 3 [hp_X]/mL |
| FORMICA RUFA | 6 [hp_X]/mL |
| SILVER | 30 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O80TY208ZW, 922OP8YUPF, 55H0W83JO5, 3M4G523W1G |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1174-1 | Astragalus Formica | 1 mL in 1 AMPULE | LIQUID | 1 | | 7 |
| 48951-1174-1 | Astragalus Formica | 10 in 1 BOX | LIQUID | 10 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1174 | ASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.] | 6 | Current NDC, Legacy NDC, 2 package rows | 20241127_63230d4e-9c45-4d1e-83c9-80df269a6c3d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1174-1 | 48951117401 | 10 AMPULE in 1 BOX (48951-1174-1) / 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |