DENDROPANAX M- red ginseng pill

DENDROPANAX M by

Drug Labeling and Warnings

DENDROPANAX M by is a Otc medication manufactured, distributed, or labeled by Inc MBG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Chew one pill thoroughly once a day

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

for oral use only

WARNINGS

Do not use this product if the expiration date has passed

Hypersensitive reactions may occur for people with special needs and/or allergies. Please check the ingredients before intake

When opening the product and/or during intake, please be careful as you may get hurt from the packaging

Avoid direct sunlight and humid areas. Store and distribute in a cool area.

PURPOSE

Dendropanax-M contains essential minerals such as Ca, K, P, Mg, S and rich saponin which need more than 100 ml per day and can help to improve immunity and blood circulation. Red ginseng, antler, and corn oil promote recovery and physiological activity to maintain physical strength and help prevent aging. It is a healthy food for both men and women

INACTIVE INGREDIENT

Korean Dendropanax 18%,

Deer antlers 2%,

Korean Raspberry 5%,

Omija 5%,

Corni 6%,

Sealwort 10%,

Sericea lespedeza 2%,

Paecilomyces japonica 5%,

Gastrodia 5%,

Cynanchumwilfordii 5%,

Mint 5%,

Barrenwort 2%,

Honey

ACTIVE INGREDIENT

red ginseng

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DENDROPANAX M 
red ginseng pill

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70694-0004
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PANAX GINSENG WHOLE (UNII: 9L5JEP7MES) (PANAX GINSENG WHOLE - UNII:9L5JEP7MES)	PANAX GINSENG WHOLE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
RASPBERRY (UNII: 4N14V5R27W)
HONEY (UNII: Y9H1V576FH)

Product Characteristics
Color	brown	Score	no score
Shape	ROUND	Size	15mm
Flavor		Imprint Code	none
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70694-0004-1	45 g in 1 BOX; Type 0: Not a Combination Product	01/24/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/24/2019

Labeler - Inc MBG (688436167)

Establishment
Name	Address	ID/FEI	Business Operations
Inc MBG		688436167	manufacture(70694-0004)