Label: GMW-GOLD- zeolite liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74651-0001-1 - Packager: DONGBO BIO CO.,LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated January 14, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
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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
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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
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GMW-GOLD
zeolite liquidProduct 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)