G-4- alnus glutinosa leaf solution

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

ALNUS GLUTINOSA LEAF (UNII: 83F04L6KZ4) (ALNUS GLUTINOSA LEAF - UNII:83F04L6KZ4)

Available from:

DNA Labs, Inc.

Administration route:

SUBLINGUAL

Prescription type:

OTC DRUG

Therapeutic indications:

Migraines, heartburn, support for adrenal glands, joint stiffness.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

G-4- ALNUS GLUTINOSA LEAF SOLUTION
DNA LABS, INC.
_Disclaimer: This homeopathic product has not been evaluated by the
Food and Drug Administration for safety_
_or efficacy. FDA is not aware of scientific evidence to support
homeopathy as effective._
----------
G-4
NDC 58264-0367-2
INDICATIONS
Migraines, heartburn, support for adrenal glands, joint stiffness.
INGREDIENTS
ACTIVE
Alnus glutinosa (Alder) 1DH
INACTIVE
36.6% alcohol (V/V) Glycerin Macerate
SUGGESTED DOSAGE
One dropper full twice daily.
SHAKE WELL
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.
To be used according to standard homeopathic indications.
PRINCIPAL DISPLAY PANEL - 2 FL. OZ. BOTTLE LABEL
DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.
G-4
ALNUS
GLUTINOSA
GEMMOTHERAPY
2 FL. OZ.
G-4
alnus glutinosa leaf solution
DNA Labs, Inc.
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:58264-0367
ROUTE OF ADMINISTRATION
SUBLINGUAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALNUS GLUTINOSA LEAF (UNII: 83F04L6KZ4) (ALNUS GLUTINOSA LEAF -
UNII:83F04L6KZ4)
ALNUS GLUTINOSA LEAF
1 [hp_X] in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1 NDC:58264-0367-2
59.14 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
01/01/1990
MARKETING INFORMATION
MARKETING CATEGORY
APPLICATION NUMBER OR MONOGRAPH CITATION
MARKETING START DATE
MARKETING END DATE
unapproved homeopathic
01/01/1990
LABELER -
DNA Labs, Inc. (031784339)
Revised: 6/2022