Lapis albus is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Calcium Hexafluorosilicate.
| Product ID | 68428-468_75ce2c41-4a13-127a-e053-2a91aa0a1e7b |
| NDC | 68428-468 |
| Product Type | Human Otc Drug |
| Proprietary Name | Lapis albus |
| Generic Name | Calcium Hexafluorosilicate |
| Dosage Form | Pellet |
| 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]/1 |
| 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 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-05-14 |
| Ingredient | Strength |
|---|---|
| CALCIUM HEXAFLUOROSILICATE | 30 [hp_C]/1 |
| SPL SET ID: | 8caee9f0-724b-4382-b904-e946938ff1eb |
| 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 |