Fluorite
- Product NDC
- 63083-8118
- 11-digit product format
- 630838118
- Labeler code
- 63083
- Product ID
- 63083-8118_683cd94d-7bf4-4ba4-b90b-8df1fda07995
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fluorite
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Substance
- CALCIUM FLUORIDE
- Active strength
- 6 [hp_X]/59mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fluorite
- Brand name suffix
- 8118
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM FLUORIDE | 6 [hp_X]/59mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O3B55K4YKI |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63083-8118-2 | Fluorite8118 | 59 mL in 1 BOTTLE, DROPPER | LIQUID | 59 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-8118 | FLUORITE 8118 (FLUORITE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220217_27d3a249-494b-4783-9e08-808296c7b2d2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-8118-2 | 63083811802 | 59 mL in 1 BOTTLE, DROPPER (63083-8118-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |