NDC 0220-3053

Lapis albus

Calcium Hexafluorosilicate

Lapis albus is a Oral Pellet in the Human Prescription Drug category. It is labeled and distributed by Boiron. The primary component is Calcium Hexafluorosilicate.

• Product ID: 0220-3053_68f897e3-b392-1cca-e053-2a91aa0ae21d
• NDC: 0220-3053
• Product Type: Human Prescription Drug
• Proprietary Name: Lapis albus
• Generic Name: Calcium Hexafluorosilicate
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: CALCIUM HEXAFLUOROSILICATE
• Active Ingredient Strength: 6 [hp_C]/6[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-3053-41

6 [hp_C] in 1 TUBE (0220-3053-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-3053-41 [00220305341]

Lapis albus PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
CALCIUM HEXAFLUOROSILICATE	6 [hp_C]/6[hp_C]

OpenFDA Data

• SPL SET ID: 68f897e3-b391-1cca-e053-2a91aa0ae21d
• Manufacturer:
  • Boiron
• UNII:
  • 2NVP93XVQ3

NDC Crossover Matching brand name "Lapis albus" or generic name "Calcium Hexafluorosilicate"

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