T-9- clematis vitalba whole solution

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Buy It Now

Active ingredient:

CLEMATIS VITALBA WHOLE (UNII: 7PH07Z124Q) (CLEMATIS VITALBA WHOLE - UNII:7PH07Z124Q)

Available from:

DNA Labs, Inc.

Administration route:

SUBLINGUAL

Prescription type:

OTC DRUG

Therapeutic indications:

Indifference, dreaminess, inattention, unconsciousness.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

                                T-9- CLEMATIS VITALBA WHOLE 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._
----------
T-9
NDC 58264-0254-1
INDICATIONS
Indifference, dreaminess, inattention, unconsciousness.
INGREDIENTS
ACTIVE
Clematis vitalba 6/8/30x
INACTIVE
20% alcohol in purified water.
SUGGESTED DOSAGE
One dropper under tongue two times daily. Acute symptoms ½ dropper
under tongue
every 30 minutes for two hours.
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 - 1 FL. OZ. BOTTLE LABEL
DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.
T-9
CLEMATIS
FLOWER ESSENCES
1 FL. OZ.
T-9
clematis vitalba whole solution
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:58264-0254
ROUTE OF ADMINISTRATION
SUBLINGUAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
CLEMATIS VITALBA WHOLE (UNII: 7PH07Z124Q) (CLEMATIS VITALBA WHOLE -
UNII:7PH07Z 124Q)
CLEMATIS VITALBA
WHOLE
30 [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
DNA Labs, Inc.
1
NDC:58264-
0254-1
29.57 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: 5/2022
                                
                                Read the complete document
                                
                            

Search alerts related to this product