GMW-GOLD- zeolite liquid

GMW-Gold by

Drug Labeling and Warnings

GMW-Gold by is a Otc medication manufactured, distributed, or labeled by DONGBO BIO CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

zeolite

INACTIVE INGREDIENT

Water, calcium, chitosan acid, iodine potassium

PURPOSE

Air Freshener

Eliminate Virus

Effective in Bird flu and Newcastle disease

Effective in foot & mouth disease, brucellosis, hog cholera and classical swine fever.

Be extinct Zika virus

Red tide and green tide treatment

Water purification

Natural ingredients for cosmetics

Sick house syndrome treatment

Additives for functional plastic, fiber and freshness box

WARNINGS

■ if following abnormal symptoms persist, discontinue use

Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes

■ Stop immediately and consult a doctor if you experience

1) Hypersensitivity symptoms such as erythema, itching and dermatitis.

2) Skin Irritation

3) Following Instructions when using medication

(1) For external use only (Do not use internally)

(2) Avoid getting into the eyes (if contact occurs, wash well with clean water)

■ Be careful not to inhale or use excessively for a long time (ingesting ethanol repeatedly causes irritation to mucous membranes and headaches or other symptoms may appear. When used repeatedly in the same area, skin irritation may occur.

■ Do not use the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin.

It is not recommended to use this one areas that have been medically treated with a cast or bandage.

■ Do not use in combination with soap or antibacterial cleansing agents.

KEEP OUT OF REACH OF CHILDREN

Keep Out of Reach of Children.

INDICATIONS & USAGE

■ spray a small amount into hands, spread evenly and rub into the skin

DOSAGE & ADMINISTRATION

for topical use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GMW-GOLD 
zeolite liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74651-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZEOLITE A (UNII: Y3NG9WF08W) (ZEOLITE A - UNII:Y3NG9WF08W)	ZEOLITE A	9.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CALCIUM (UNII: SY7Q814VUP)
CHITOSAN OLIGOSACCHARIDE (UNII: 23R93M6Y64)
IODINE (UNII: 9679TC07X4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74651-0001-1	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/04/2020

Labeler - DONGBO BIO CO.,LTD (693901450)

Registrant - DONGBO BIO CO.,LTD (693901450)

Establishment
Name	Address	ID/FEI	Business Operations
DONGBO BIO CO.,LTD		693901450	manufacture(74651-0001)