Label: IBREA MICRO SILVER ANTI BACTERIAL WITH PURE SILVER- silver spray
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Contains inactivated NDC Code(s)
NDC Code(s): 78030-040-01 - Packager: IBREA GLOBAL 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 July 9, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENTS
- PURPOSE
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WARNINGS
For external use only.
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Do not use
• On children less than 2 months of age.
• Avoid contact with broken skin.
• Avoid contact with metallic items.
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if skin irritation occurs and consult a doctor immediately. - KEEP OUT OF REACH OF CHILDREN
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Uses
This anti-bacterial spray provides an anti-microbial protection film on surfaces and environment. It also refreshes and reduces bacterial growth through silver ions released from MicroSilver BG™, which is pure metallic silver with a highly porous structure and continuously releases active silver ions to inhibit bacterial growth on the surface of the skin.
MicroSilver BG™ has been certified as natural and organic in the EU & the USA and is safe for humans and the environment. - Directions
- Other information
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
IBREA MICRO SILVER ANTI BACTERIAL WITH PURE SILVER
silver sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78030-040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 0.098 g in 98 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) BETASIZOFIRAN (UNII: 2X51AD1X3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78030-040-01 98 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2020 Labeler - IBREA GLOBAL CO.,LTD. (694812182) Registrant - IBREA GLOBAL CO.,LTD. (694812182) Establishment Name Address ID/FEI Business Operations Mi-face Co., Ltd 694820628 manufacture(78030-040)
