FDA.reportPublic FDA data

The Cell Salt Co. Daily Blend 12 in 1

Product NDC
87674-100
Requested package NDC
87674-100-10
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
IngredientStrength
FERROSOFERRIC PHOSPHATE12 [hp_X]/1
SODIUM SULFATE6 [hp_X]/1
CALCIUM SULFATE ANHYDROUS6 [hp_X]/1
CALCIUM FLUORIDE12 [hp_X]/1
SILICON DIOXIDE12 [hp_X]/1
POTASSIUM CHLORIDE6 [hp_X]/1
SODIUM CHLORIDE6 [hp_X]/1
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE6 [hp_X]/1
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE6 [hp_X]/1
POTASSIUM PHOSPHATE6 [hp_X]/1
POTASSIUM SULFATE6 [hp_X]/1
TRIBASIC CALCIUM PHOSPHATE6 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 12 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
91GQH8I5F7Internal UNII lookup
0YPR65R21JInternal UNII lookup
E934B3V59HInternal UNII lookup
O3B55K4YKIInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
660YQ98I10Internal UNII lookup
451W47IQ8XInternal UNII lookup
HF539G9L3QInternal UNII lookup
70WT22SF4BInternal UNII lookup
B7862WZ632Internal UNII lookup
1K573LC5TVInternal UNII lookup
91D9GV0Z28Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
55826f59-acf4-7370-e063-6394a90afed7Available on FDA.report

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
The Cell Salt Co. Daily Blend 12 in 1CALC FLUOR, CALC PHOS, CALC SULPH, FERRUM PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT MUR, NAT PHOS, NAT SULPH, SILICEAThe Cell Salt Company LLC55826f59-acf4-7370-e063-6394a90afed72026-07-01WarningsExact identifier
ndc (package): 87674-100-10
ndc (product): 87674-100
ndc11 (package): 87674010010

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
87674-100-1087674010010400 TABLET, SOLUBLE in 1 BOTTLE (87674-100-10) 2026-07-01NoNoCurrent