Home NDC 68703-355-80 AmazaPet
Product NDC 68703-355
Requested package NDC 68703-355-80
11-digit product format 687030355
Labeler code 68703
Product ID 68703-355_4e4a2296-f5d2-4c2d-9b53-676cc9d9b6cc
Type HUMAN OTC DRUG
Nonproprietary name Althaea, Arsenicum alb, Inula, Kali mur, Mag phos
Dosage form TABLET
Route ORAL
Labeler SILVER STAR BRANDS
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-01-04
Substance ALTHAEA OFFICINALIS LEAF; ARSENIC TRIOXIDE; INULA HELENIUM WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PHOSPHORUS; POTASSIUM CHLORIDE
Active strength 6; 30; 6; 8; 30; 6 [hp_X]/1801; [hp_C]/1801; [hp_X]/1801; [hp_X]/1801; [hp_C]/1801; [hp_X]/1801
Pharmacologic classes Calculi Dissolution Agent [EPC], 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 Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 11 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Additional Listing Data#
Finished product Yes
Brand name base AmazaPet
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM CHLORIDE 6 [hp_X]/1801 MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 30 [hp_C]/1801 ARSENIC TRIOXIDE 6 [hp_X]/1801 INULA HELENIUM WHOLE 8 [hp_X]/1801 ALTHAEA OFFICINALIS LEAF 30 [hp_C]/1801 PHOSPHORUS 6 [hp_X]/1801
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68703-355-80 AmazaPet 180 in 1 BOTTLE, GLASS TABLET 180 4
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 Marketing end Sample Exclude flag Status 68703-355-80 68703035580 180 TABLET in 1 BOTTLE, GLASS (68703-355-80) 180 tablet 2021-01-04 0000-00-00 No No Current