Home NDC 87835-103 Bio Combination 28
Product NDC 87835-103
11-digit product format 878350103
Labeler code 87835
Product ID 87835-103_597caf33-5108-9dec-e063-6294a90a5fcd
Type HUMAN OTC DRUG
Nonproprietary name Schuessler Salts
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler LDD Bioscience Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-08-20
Substance CALCIUM FLUORIDE; CALCIUM PHOSPHATE; FERROUS PHOSPHATE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; MAGNESIUM PHOSPHATE; SODIUM CHLORIDE; SODIUM PHOSPHATE; SODIUM SULFATE; SILICON DIOXIDE; CALCIUM SULFATE; POTASSIUM PHOSPHATE
Active strength 37.5; 37.5; 37.5; 37.5; 37.5; 37.5; 37.5; 37.5; 37.5; 37.5; 37.5; 37.5 g/450g; g/450g; g/450g; g/450g; g/450g; g/450g; g/450g; g/450g; g/450g; g/450g; g/450g; g/450g
Pharmacologic classes Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [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], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Bio Combination 28
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM FLUORIDE 37.5 g/450g CALCIUM PHOSPHATE 37.5 g/450g FERROUS PHOSPHATE 37.5 g/450g POTASSIUM CHLORIDE 37.5 g/450g POTASSIUM SULFATE 37.5 g/450g MAGNESIUM PHOSPHATE 37.5 g/450g SODIUM CHLORIDE 37.5 g/450g SODIUM PHOSPHATE 37.5 g/450g SODIUM SULFATE 37.5 g/450g SILICON DIOXIDE 37.5 g/450g CALCIUM SULFATE 37.5 g/450g POTASSIUM PHOSPHATE 37.5 g/450g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87835-103-01 87835010301 450 g in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (87835-103-01) 450 g 2026-08-20 No No Current