ULMUS GLABRA WHOLE

FDA Drug Profile — G-41

ULMUS GLABRA WHOLE is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including G-41. Available dosage form: solution.

Drug Details

Generic Name
ULMUS GLABRA WHOLE
Brand Names
G-41
Application Number
Sponsor
DNA Labs, Inc.
NDC Codes
1
Dosage Forms
SOLUTION
Routes
SUBLINGUAL
Active Ingredients
ULMUS GLABRA WHOLE

Indications and Usage

INDICATIONS Support for the joints and skin.

Warnings

Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.