Label: V3 VIRAL DEFENSE NANO SILVER SKIN AND SURFACE PROTECTANT- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 79518-030-01, 79518-030-02, 79518-030-03, 79518-030-04, view more79518-030-05 - Packager: Core Pacific, Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 10, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DRUG FACTS
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS:
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
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SPL UNCLASSIFIED SECTION
• NON-ALCOHOL
• APPLICABLE ON ALL SURFACES
• GUARDS AGAINST INFECTION
• ECO-FRIENDLY
99.99% EFFECTIVE AGAINST BACTERIA, VIRUSES & MOST COMMON GERMS.
24 HOURS SKIN PROTECTION
30 DAY SURFACE PROTECTION
POWERED BY: V3 PROPRIETARY TECHNOLOGY
Manufactured by:
Core Pacific, Inc. for
V3 International Inc.
4000 Leeland St
Houston, TX 77023
www.v3viraldefense.com
1-888-462-4928
MADE IN USA.
- Packaging
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INGREDIENTS AND APPEARANCE
V3 VIRAL DEFENSE NANO SILVER SKIN AND SURFACE PROTECTANT
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79518-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SILVER (UNII: 3M4G523W1G) .GAMMA.-METHACRYLOXYPROPYLTRIMETHOXYSILANE (UNII: JV48X1M2EQ) SODIUM SESQUICARBONATE (UNII: Y1X815621J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79518-030-01 59.14 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/01/2020 2 NDC:79518-030-02 250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/01/2020 3 NDC:79518-030-03 1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/01/2020 4 NDC:79518-030-04 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/01/2020 5 NDC:79518-030-05 208198 mL in 1 DRUM; Type 0: Not a Combination Product 08/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/01/2020 Labeler - Core Pacific, Inc. (022106593) Establishment Name Address ID/FEI Business Operations Core Pacific, Inc. 022106593 manufacture(79518-030)
