GMW VITAPET: Product Information

GMW VITAPET- 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.


alcium, bentonite, chitosan, potassium Iodide, muscovite, dimethyl sulphone, sodium molybdate, purified water

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 the animal, spread evenly and rub into the skin

for topical use only

(click image for full-size original)

zeolite liquid
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:74651-0008
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:74651-0008-1 1000 mL in 1 BOTTLE, SPRAY None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/27/2022
Labeler — DONGBO BIO CO.,LTD (693901450)
Name Address ID/FEI Operations
DONGBO BIO CO.,LTD 693901450 manufacture, api manufacture

Revised: 05/2022 DONGBO BIO CO.,LTD provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by Every individual animal healthcare product label entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

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