Colchicum autumnale pellet

Active ingredient

COLCHICUM AUTUMNALEHPUS 3X and higher

Uses

Neuritis Of Limbs

Indications

Condition listed above or as directed by the physician

Dosage

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

Warnings

This product is to be used for self-limiting conditions

Otc - stop use section

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

Otc - pregnancy or breast feeding section

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

Otc - keep out of reach of children section

Keep this and all medication out of reach of children

Otc - do not use section

Do not use if capseal is broken or missing.

Close the cap tightly after use.

Inactive ingredients

Sucrose

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

Ingredients and appearance - Product information

Colchicum autumnale pellet- Colchicum autumnale

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 15631-0150
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Colchicum autumnale bulb ( UNII: 993QHL78E6)( Colchicum autumnale bulb - UNII: 993QHL78E6 ) 3 [hp_X]in 1

Inactive Ingredients

Ingredient Name Code
Sucrose ( UNII: C151H8M554)

Product Characteristics

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 15631-0150-0 100 in 1 PACKAGE 2018/01/01
2 NDC: 15631-0150-1 200 in 1 PACKAGE 2018/01/01
3 NDC: 15631-0150-2 400 in 1 PACKAGE 2018/01/01
4 NDC: 15631-0150-3 750 in 1 PACKAGE 2018/01/01
5 NDC: 15631-0150-4 2500 in 1 PACKAGE 2018/01/01
6 NDC: 15631-0150-5 12500 in 1 PACKAGE 2018/01/01

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
unapproved homeopathic USA 2018/01/01

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

Establishment

Name ID/FEI Business Operations
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc 650833994 manufacture( 15631-0150), label( 15631-0150)

Package label.principal display panel