Reflux

Product NDC
43742-1606
Requested package NDC
43742-1606-1
11-digit product format
437421606
Labeler code
43742
Product ID
43742-1606_f656d753-8672-4695-94fd-d674823c6cde
Type
HUMAN OTC DRUG
Nonproprietary name
Adenosinum Triphosphoricum Dinatrum, Nadidum, Argentum Nitricum, Robinia Pseudoacacia, Sulphur, Origanum Vulgare, Duodenum (Suis), Esophagus (Suis), Funiculus Umbilicalis Suis, Stomach (Suis), Nux Vomica, Coumarinum, Pancreatinum, Muriaticum Acidum, Citricum Acidum, Formicum Acidum, Sarcolacticum Acidum, Coenzyme A, Proteus (Morgani)
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-11-04
Marketing end
2024-12-02
Substance
ADENOSINE TRIPHOSPHATE DISODIUM; NADIDE; SILVER NITRATE; ROBINIA PSEUDOACACIA BARK; SULFUR; OREGANO; SUS SCROFA DUODENUM; SUS SCROFA ESOPHAGUS; SUS SCROFA UMBILICAL CORD; SUS SCROFA STOMACH; STRYCHNOS NUX-VOMICA SEED; COUMARIN; PANCRELIPASE; HYDROCHLORIC ACID; ANHYDROUS CITRIC ACID; FORMIC ACID; LACTIC ACID, L-; COENZYME A; PROTEUS MORGANII
Active strength
6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage43742-160643742-1606-1DDiscontinued by firm2026-08-03

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 · 9 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1606-14374216060130 mL in 1 BOTTLE, DROPPER (43742-1606-1) 30 ml2019-11-042024-12-02NoNoCurrent