DIGITALIS PURPUREA tablet

DIGITALIS PURPUREA by

Drug Labeling and Warnings

DIGITALIS PURPUREA by is a Homeopathic medication manufactured, distributed, or labeled by Rxhomeo Private Limited d.b.a. Rxhomeo, Inc, Rxhomeo, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DIGITALIS PURPUREA HPUS 6X and Higher

USES

Swollen Legs

INDICATIONS

Condition listed above or as directed by the physician

DOSAGE

Adults- Take 4 or 6 Tablets by mouth, three times daily or as suggested by physician. Children 2 years and older- take 1/2 the adult dose.

WARNINGS

This product is to be used for self-limiting conditions

If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional

As with any drug, if you are pregnant, or nursing a baby, seek professional advice before taking this product

Keep this and all medication out of reach of children

Do not use if capseal is broken or missing.

Close the cap tightly after use.

INACTIVE INGREDIENTS

Lactose

STORAGE

Store in a cool dark place

QUESTIONS OR COMMENTS

www.Rxhomeo.com | 1.888.2796642 | info@rxhomeo.com

Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DIGITALIS PURPUREA 
digitalis purpurea tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 15631-0573
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B)	DIGITALIS	6 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	3mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 15631-0573-0	1 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 15631-0573-1	4 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC: 15631-0573-2	50 in 1 CONTAINER; Type 0: Not a Combination Product
4	NDC: 15631-0573-3	100 in 1 CONTAINER; Type 0: Not a Combination Product
5	NDC: 15631-0573-4	250 in 1 CONTAINER; Type 0: Not a Combination Product
6	NDC: 15631-0573-5	500 in 1 CONTAINER; Type 0: Not a Combination Product
7	NDC: 15631-0573-6	1000 in 1 CONTAINER; Type 0: Not a Combination Product
8	NDC: 15631-0573-7	10000 in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/27/2015

Labeler - Rxhomeo Private Limited d.b.a. Rxhomeo, Inc (650833994)

Establishment
Name	Address	ID/FEI	Business Operations
Rxhomeo, Inc		832534981	wholesale drug distributor(15631-0573)

Establishment
Name	Address	ID/FEI	Business Operations
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc		650833994	manufacture(15631-0573) , label(15631-0573)