FDA.reportPublic FDA data

Guaiacum

Product NDC
71919-328
11-digit product format
719190328
Labeler code
71919
Product ID
71919-328_7e4f6f6b-c0a5-c1ff-e053-2a91aa0a5f70
Type
HUMAN OTC DRUG
Nonproprietary name
GUAIACUM OFFICINALE RESIN
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-04-01
Marketing end
0000-00-00
Substance
GUAIACUM OFFICINALE RESIN
Active strength
30 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 5 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71919-328DDiscontinued by firm2026-08-03
excluded packagepackage71919-32871919-328-07DDiscontinued by firm2026-08-03
excluded packagepackage71919-32871919-328-08DDiscontinued by firm2026-08-03
excluded packagepackage71919-32871919-328-09DDiscontinued by firm2026-08-03
excluded packagepackage71919-32871919-328-10DDiscontinued by firm2026-08-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-328-077191903280715 mL in 1 VIAL, GLASS (71919-328-07) 15 ml2010-04-010000-00-00NoNoCurrent
71919-328-087191903280830 mL in 1 VIAL, GLASS (71919-328-08) 30 ml2010-04-010000-00-00NoNoCurrent
71919-328-097191903280950 mL in 1 BOTTLE, GLASS (71919-328-09) 50 ml2010-04-010000-00-00NoNoCurrent
71919-328-1071919032810100 mL in 1 BOTTLE, GLASS (71919-328-10) 100 ml2010-04-010000-00-00NoNoCurrent