Lapis albus is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Calcium Hexafluorosilicate.
Product ID | 71919-403_7e5682b5-9b2b-9b4d-e053-2991aa0a71fc |
NDC | 71919-403 |
Product Type | Human Otc Drug |
Proprietary Name | Lapis albus |
Generic Name | Calcium Hexafluorosilicate |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2010-05-14 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Washington Homeopathic Products |
Substance Name | CALCIUM HEXAFLUOROSILICATE |
Active Ingredient Strength | 30 [hp_C]/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2010-05-14 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-05-14 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-05-14 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-05-14 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-05-14 |
Ingredient | Strength |
---|---|
CALCIUM HEXAFLUOROSILICATE | 30 [hp_C]/mL |
SPL SET ID: | fc3e6431-e455-4e2a-a41b-5b875e9dcd2c |
Manufacturer | |
UNII | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0220-3053 | Lapis albus | CALCIUM HEXAFLUOROSILICATE |
0220-3055 | Lapis albus | CALCIUM HEXAFLUOROSILICATE |
15631-0266 | LAPIS ALBUS | LAPIS ALBUS |
68428-468 | Lapis albus | CALCIUM HEXAFLUOROSILICATE |
71919-403 | Lapis albus | CALCIUM HEXAFLUOROSILICATE |
64117-251 | ITCHING SKIN | CALCIUM HEXAFLUOROSILICATE |