Home NDC 87674-100 The Cell Salt Co. Daily Blend 12 in 1
Product NDC 87674-100
11-digit product format 876740100
Labeler code 87674
Product ID 87674-100_558261cb-4904-6f03-e063-6394a90a58e1
Type HUMAN OTC DRUG
Nonproprietary name Calc Fluor, Calc Phos, Calc Sulph, Ferrum Phos, Kali Mur, Kali Phos, Kali Sulph, Mag Phos, Nat Mur, Nat Phos, Nat Sulph, Silicea
Dosage form TABLET, SOLUBLE
Route ORAL
Labeler The Cell Salt Company LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-07-01
Substance FERROSOFERRIC PHOSPHATE; SODIUM SULFATE; CALCIUM SULFATE ANHYDROUS; CALCIUM FLUORIDE; SILICON DIOXIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; POTASSIUM PHOSPHATE; POTASSIUM SULFATE; TRIBASIC CALCIUM PHOSPHATE
Active strength 12; 6; 6; 12; 12; 6; 6; 6; 6; 6; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], 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], 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 Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], 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 The Cell Salt Co. Daily Blend 12 in 1
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FERROSOFERRIC PHOSPHATE 12 [hp_X]/1 SODIUM SULFATE 6 [hp_X]/1 CALCIUM SULFATE ANHYDROUS 6 [hp_X]/1 CALCIUM FLUORIDE 12 [hp_X]/1 SILICON DIOXIDE 12 [hp_X]/1 POTASSIUM CHLORIDE 6 [hp_X]/1 SODIUM CHLORIDE 6 [hp_X]/1 MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 6 [hp_X]/1 SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 6 [hp_X]/1 POTASSIUM PHOSPHATE 6 [hp_X]/1 POTASSIUM SULFATE 6 [hp_X]/1 TRIBASIC CALCIUM PHOSPHATE 6 [hp_X]/1
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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join The Cell Salt Co. Daily Blend 12 in 1 CALC FLUOR, CALC PHOS, CALC SULPH, FERRUM PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT MUR, NAT PHOS, NAT SULPH, SILICEA The Cell Salt Company LLC 55826f59-acf4-7370-e063-6394a90afed7 2026-07-01 Warnings Exact identifier ndc (product): 87674-100
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 87674-100-10 87674010010 400 TABLET, SOLUBLE in 1 BOTTLE (87674-100-10) 2026-07-01 No No Current