DIGITALIS PUPUREA- digitalis pellet

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

DIGITALIS

Available from:

Washington Homeopathic Products

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

To relieve the symptoms of worry. Indications: DIGITALIS Worry If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

                                DIGITALIS PUPUREA - DIGITALIS PELLET
WASHINGTON HOMEOPATHIC PRODUCTS
_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._
----------
DRUG FACTS
ACTIVE INGREDIENTS
DIGITALIS
USES
To relieve the symptoms of worry.
KEEP OUT OF REACH OF CHILDREN
Keep this and all medicines out of reach of children.
INDICATIONS
Indications:
DIGITALIS Worry
STOP USE AND ASK DOCTOR
If symptoms persist/worsen or if pregnant/nursing, stop use and
consult your
practitioner.
DIRECTIONS
Adults: Dissolve 3 to 5 under the tongue three times a day or as
directed by Lic.
Practitioner. Take at greater intervals as condition subsides.
Children: Dissolve 3 to 5
under the tongue three times a day or as directed by Lic.
Practitioner. Take at greater
intervals as condition subsides.
INACTIVE INGREDIENTS
Sucrose/Lactose
PRINCIPAL DISPLAY PANEL
The OTC potency range of DIGITALIS is 4x–30x, 2c–30c, 200c, 1m,
10m, 50m, and CM.
Availability is subject to change.
All WHP single remedies are made to order; thus, the labels are
printed on the same
label stock as the orders are filled.
‘Bottle Size’ and ‘Potency’ vary on the label depending on
customer choice.
Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1
ounce, 2 ounce,
and 4 ounce.
DIGITALIS PUPUREA
digitalis pellet
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:68428-357
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B)
DIGITALIS
30 [hp_C]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
SUCROSE (UNII: C151H8M554)
LACTOSE (UNII: J2B2A4N98G)
PRODUCT CHARACTERISTICS
COLOR
white (white)
SCORE
SHAPE
SIZE
FLAVOR
IMPRINT CODE
CONTAINS
Washington Homeopathic Products
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:68428-
357-03
75 in 1 VIAL, GLASS; Type 0: Not a 
                                
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