Home NDC 68703-395 NativeRemedies Triple Complex UT Tonic
Product NDC 68703-395
11-digit product format 687030395
Labeler code 68703
Product ID 68703-395_2ab123a4-1043-63f4-e063-6394a90a9bab
Type HUMAN OTC DRUG
Nonproprietary name Ferrum phos, Kalii sulph, Nat phos.
Dosage form LIQUID
Route ORAL
Labeler Silver Star Brands
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-04-03
Substance POTASSIUM SULFATE; FERROSOFERRIC PHOSPHATE; SODIUM PHOSPHATE, DIBASIC
Active strength 6; 8; 6 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 NativeRemedies Triple Complex UT Tonic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM SULFATE 6 [hp_X]/59mL FERROSOFERRIC PHOSPHATE 8 [hp_X]/59mL SODIUM PHOSPHATE, DIBASIC 6 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1K573LC5TV Internal UNII lookup 91GQH8I5F7 Internal UNII lookup GR686LBA74 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68703-395-02 NativeRemedies Triple Complex UT Tonic 59 mL in 1 BOTTLE, GLASS LIQUID 59 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68703-395 NATIVEREMEDIES TRIPLE COMPLEX UT TONIC (FERRUM PHOS, KALII SULPH, NAT PHOS.) LIQUID [SILVER STAR BRANDS] 3 Current NDC, 1 package rows 20250103_f78009d0-af67-4b5a-e053-6294a90ac55b.zip
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 68703-395-02 68703039502 59 mL in 1 BOTTLE, GLASS (68703-395-02) 59 ml 2023-04-03 No No Current