Bestmade Natural Products BIO20 Lactose Free

Product NDC
82969-8020
11-digit product format
829698020
Labeler code
82969
Product ID
82969-8020_30394e7e-1710-7b9d-e063-6394a90afcdb
Type
HUMAN OTC DRUG
Nonproprietary name
Calc Fluor, Calc Sulph, Kali Sulph, Nat Mur, Nat Sulph
Dosage form
TABLET, SOLUBLE
Route
ORAL
Labeler
Bestmade Natural Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-01-01
Substance
CALCIUM FLUORIDE; CALCIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM CHLORIDE; SODIUM SULFATE
Active strength
6; 6; 6; 6; 6 [hp_X]/6[hp_X]; [hp_X]/6[hp_X]; [hp_X]/6[hp_X]; [hp_X]/6[hp_X]; [hp_X]/6[hp_X]
Pharmacologic classes
Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
O3B55K4YKICALCIUM FLUORIDE7789-75-5CALCIUM FLUORIDE
E934B3V59HCALCIUM SULFATE ANHYDROUS7778-18-9CALCIUM SULFATE ANHYDROUS
1K573LC5TVPOTASSIUM SULFATE7778-80-5POTASSIUM SULFATE
451W47IQ8XSODIUM CHLORIDE7647-14-5SODIUM CHLORIDE
0YPR65R21JSODIUM SULFATE7727-73-3SODIUM SULFATE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
82969-8020-1829698020016 [hp_X] in 1 BOTTLE, GLASS (82969-8020-1) 2015-01-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
BIO20 Hair, Nails & Skin Solutions* LACTOSE FREE Sugar Cane BaseBestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro2025-03-13HUMAN OTC DRUG LABEL1