NDC 0220-3055

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 ID0220-3055_861bb302-0d93-0aa2-e053-2a91aa0a52cf
NDC0220-3055
Product TypeHuman Prescription Drug
Proprietary NameLapis albus
Generic NameCalcium Hexafluorosilicate
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date1983-03-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBoiron
Substance NameCALCIUM HEXAFLUOROSILICATE
Active Ingredient Strength9 [hp_C]/9[hp_C]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0220-3055-41

9 [hp_C] in 1 TUBE (0220-3055-41)
Marketing Start Date1983-03-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0220-3055-41 [00220305541]

Lapis albus PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1983-03-03

Drug Details

Active Ingredients

IngredientStrength
CALCIUM HEXAFLUOROSILICATE9 [hp_C]/9[hp_C]

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

NDCBrand NameGeneric Name
0220-3053Lapis albusCALCIUM HEXAFLUOROSILICATE
0220-3055Lapis albusCALCIUM HEXAFLUOROSILICATE
15631-0266LAPIS ALBUSLAPIS ALBUS
68428-468Lapis albusCALCIUM HEXAFLUOROSILICATE
71919-403Lapis albusCALCIUM HEXAFLUOROSILICATE
64117-251ITCHING SKINCALCIUM HEXAFLUOROSILICATE

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.