Chronagesic

Product NDC
43742-1273
11-digit product format
437421273
Labeler code
43742
Product ID
43742-1273_02cfc91a-856d-4fb2-8520-f7e43526e960
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Montana, Cinnamomum, Dulcamara, Funiculus Umbilicalis Suis, Nadidum, Natrum Oxalaceticum, Pantothenic Acid, Placenta Totalis Suis, Sanguinaria Canadensis, Sulphur, Apiolum, Piper Nigrum, Alpha-Lipoicum Acidum, Cartilago Suis, Rhus Tox, Silicea, Symphytum Officinale, Thuja Occidentalis
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-08-20
Marketing end
2025-04-21
Substance
ARNICA MONTANA; CINNAMON; SOLANUM DULCAMARA TOP; SUS SCROFA UMBILICAL CORD; NADIDE; SODIUM DIETHYL OXALACETATE; PANTOTHENIC ACID; SUS SCROFA PLACENTA; SANGUINARIA CANADENSIS ROOT; SULFUR; APIOLE (PARSLEY); GREEN PEPPERCORN; .ALPHA.-LIPOIC ACID; SUS SCROFA CARTILAGE; TOXICODENDRON PUBESCENS LEAF; SILICON DIOXIDE; COMFREY ROOT; THUJA OCCIDENTALIS LEAFY TWIG
Active strength
3 [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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct43742-1273DDiscontinued by firm2026-08-17
excluded packagepackage43742-127343742-1273-1DDiscontinued by firm2026-08-17

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 · 4 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage43742-1273-1d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage43742-1273-1f5e01cc5f278…a2eaf40c39c3…

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1273-14374212730130 mL in 1 BOTTLE, DROPPER (43742-1273-1) 30 ml2018-08-202025-04-21NoNoCurrent