Home NDC 84739-035 Jacksons Cell Salts
Product NDC 84739-035
11-digit product format 847390035
Labeler code 84739
Product ID 84739-035_54018d1b-2d0e-91ff-e063-6394a90a85ab
Type HUMAN OTC DRUG
Nonproprietary name Nat mur, Nat phos, Nat sulph
Dosage form PELLET
Route ORAL
Labeler Zettl Health Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-06-11
Substance SODIUM CHLORIDE; SODIUM SULFATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Active strength 6; 6; 6 [hp_X]/6[hp_X]; [hp_X]/6[hp_X]; [hp_X]/6[hp_X]
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 Jacksons Cell Salts
Brand name suffix DIGESTIVE BALANCE
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE 6 [hp_X]/6[hp_X] SODIUM SULFATE 6 [hp_X]/6[hp_X] SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 6 [hp_X]/6[hp_X]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 451W47IQ8X Internal UNII lookup 0YPR65R21J Internal UNII lookup 70WT22SF4B Internal UNII lookup
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 84739-035-01 84739003501 1 BOTTLE in 1 CARTON (84739-035-01) / 500 [hp_X] in 1 BOTTLE 1 bottle 2026-06-11 No No Current