GMW-Gold: Package Insert and Label Information

GMW-GOLD- zeolite a liquid

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.


Water, calcium, chitosan acid, iodine potassium

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

■ 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.

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

for topical use only


zeolite liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:74651-0001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Inactive Ingredients
Ingredient Name Strength
# Item Code Package Description Multilevel Packaging
1 NDC:74651-0001-1 1000 mL in 1 BOTTLE None
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)
Name Address ID/FEI Operations
DONGBO BIO CO.,LTD 693901450 manufacture (74651-0001)

Revised: 04/2020 DONGBO BIO CO.,LTD provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

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