Pulmo Mercurius
- Product NDC
- 48951-8425
- 11-digit product format
- 489518425
- Labeler code
- 48951
- Product ID
- 48951-8425_43e5678b-2e4f-6b11-e063-6394a90ab886
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pulmo Mercurius
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- MERCURY; SUS SCROFA LUNG
- Active strength
- 17; 8 [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pulmo Mercurius
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MERCURY | 17 [hp_X]/mL |
| SUS SCROFA LUNG | 8 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FXS1BY2PGL, 7GL3G1COB3 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-8425-3 | Pulmo Mercurius | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8425 | PULMO MERCURIUS LIQUID [URIEL PHARMACY INC.] | 5 | Current NDC, 1 package rows | 20250124_2889ec85-faab-21ab-e063-6394a90aaeda.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-8425-3 | 48951842503 | 60 mL in 1 BOTTLE, DROPPER (48951-8425-3) | 60 ml | 2009-09-01 | No | No | Historical |