Home NDC 68703-356-80 Respo-K
Product NDC 68703-356
Requested package NDC 68703-356-80
11-digit product format 687030356
Labeler code 68703
Product ID 68703-356_33e66cd2-61e0-4bd9-9b12-15f6197b4c61
Type HUMAN OTC DRUG
Nonproprietary name Calc sulph, Ferrum phos, Hepar sulph calc, Sambucus nig, Verbascum
Dosage form TABLET
Route ORAL
Labeler SILVER STAR BRANDS
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-01-04
Substance CALCIUM SULFATE; CALCIUM SULFIDE; EUROPEAN ELDERBERRY; FERROSOFERRIC PHOSPHATE; VERBASCUM THAPSUS
Active strength 6; 12; 3; 6; 3 [hp_C]/1801; [hp_C]/1801; [hp_X]/1801; [hp_C]/1801; [hp_X]/1801
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
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 Respo-K
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM SULFATE 6 [hp_C]/1801 FERROSOFERRIC PHOSPHATE 12 [hp_C]/1801 CALCIUM SULFIDE 3 [hp_X]/1801 VERBASCUM THAPSUS 6 [hp_C]/1801 EUROPEAN ELDERBERRY 3 [hp_X]/1801
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 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 68703-356-80 Respo-K 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 68703-356-80 68703035680 180 TABLET in 1 BOTTLE, GLASS (68703-356-80) 180 tablet 2021-01-04 0000-00-00 No No Current