NDC 58264-0404

G-41

Ulmus Glabra Whole

G-41 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Ulmus Glabra Whole.

Product ID58264-0404_d379a488-3f93-419d-8675-9fbf4d615964
NDC58264-0404
Product TypeHuman Otc Drug
Proprietary NameG-41
Generic NameUlmus Glabra Whole
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameULMUS GLABRA WHOLE
Active Ingredient Strength1 [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58264-0404-2

59.14 mL in 1 BOTTLE, GLASS (58264-0404-2)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0404-2 [58264040402]

G-41 SOLUTION
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ULMUS GLABRA WHOLE1 [hp_X]/mL

OpenFDA Data

SPL SET ID:9dc69a72-b1ac-4401-8c38-ccc9d775fdfc
Manufacturer
UNII

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.