Celestite 6X
- Product NDC
- 53645-1901
- 11-digit product format
- 536451901
- Labeler code
- 53645
- Product ID
- 53645-1901_1a50af81-4251-aa0d-e063-6394a90a5187
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Celestite 6X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-06-24
- Substance
- STRONTIUM SULFATE
- Active strength
- 6 [hp_X]/30mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Celestite 6X
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| STRONTIUM SULFATE | 6 [hp_X]/30mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7Q3KX2L47F |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53645-1901-6 | Celestite 6X | 30 mL in 1 BOTTLE | LIQUID | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53645-1901 | CELESTITE 6X LIQUID [TRUE BOTANICA, LLC] | 1 | Current NDC, 1 package rows | 20240703_1a50b46b-834b-bd18-e063-6394a90a58e5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53645-1901-6 | 53645190106 | 30 mL in 1 BOTTLE (53645-1901-6) | 30 ml | 2024-06-24 | No | No | Historical |