GANODERMA LUCIDUM SPORES POLYSACCHARIDES capsule

GANODERMA LUCIDUM SPORES POLYSACCHARIDES by

Drug Labeling and Warnings

GANODERMA LUCIDUM SPORES POLYSACCHARIDES by is a Otc medication manufactured, distributed, or labeled by Bestway Biomedical Technology (Shanghai) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active lngredient(in each tablet):

Active lngredient(in each tablet): Amino acids 2%, BARLEY MALT 1%

Purpose

Purpose: Promote cardiovascular and cerebrovascular health, Reaulate the immune system

Uses

Uses
Regulating immunity

Warnings

Warnings
For internal use only

Do not use

Do not use
lf you are allergic to any ingredients

When Using Section

When Using Section
When using this product, do not take other medications at the same time.
lf taking antibiotics at the same time, please interva at least 2 hours or follow medical advice.
lf discomfort occurs after consumption, please stop usingand consult a doctor.

Stop Use Section

Stop Use Section
No side effects

Keep out of reach of children

Keep out of reach of children
Children, pregnant women, and nursing mothers should not consume it

Instructions:

Instructions:
Once a day, 1 capsule each time, taken with warm water
Seal and place in a cool and dry place
This product cannot replace medication for treatment

Other information

Other information
store at 20-25°C(68-77°F)
protect from excessive moisture

lnactive ingredient.

lnactive ingredient.
GANODERMA LUCIDUM SPORES POLYSACCHARIDES

PRINCIPAL DISPLAY PANEL

83532-001-01
30 CAPSULE in 1BOX

INGREDIENTS AND APPEARANCE

GANODERMA LUCIDUM SPORES POLYSACCHARIDES 
ganoderma lucidum spores polysaccharides capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83532-001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMINO ACIDS (UNII: 0O72R8RF8A) (AMINO ACIDS - UNII:0O72R8RF8A)	AMINO ACIDS	2 g  in 9.9
BARLEY MALT (UNII: R3NBG8914U) (BARLEY MALT - UNII:R3NBG8914U)	BARLEY MALT	1 g  in 9.9

Inactive Ingredients
Ingredient Name	Strength
REISHI (UNII: TKD8LH0X2Z)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	12mm
Flavor	MALT	Imprint Code	no
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83532-001-01	30 in 1 BOX; Type 0: Not a Combination Product	06/17/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/17/2023

Labeler - Bestway Biomedical Technology (Shanghai) Co., Ltd. (699440428)

Establishment
Name	Address	ID/FEI	Business Operations
Bestway Biomedical Technology (Shanghai) Co., Ltd.		699440428	label(83532-001) , manufacture(83532-001)