Chrysolith 6X
- Product NDC
- 48951-3245
- 11-digit product format
- 489513245
- Labeler code
- 48951
- Product ID
- 48951-3245_bd474b28-bc43-08c1-e053-2995a90ae7fc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chrysolith 6X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- SILICON DIOXIDE
- Active strength
- 6 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 48951-3245-1 | Chrysolith 6X | 10 mL in 1 BOTTLE, DROPPER | LIQUID | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-3245 | CHRYSOLITH 6X LIQUID [URIEL PHARMACY INC.] | 2 | Legacy NDC, 1 package rows | 20231201_bd474b28-bc42-08c1-e053-2995a90ae7fc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-3245-1 | 48951324501 | 10 mL in 1 BOTTLE, DROPPER (48951-3245-1) | 10 ml | 2009-09-01 | 0000-00-00 | No | No | Current |