Label: DR. DU-MORES VIRAL DEFENSE NANO SILVER SKIN AND SURFACE DISINFECTANT PROTECTANT- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 79518-800-01, 79518-800-02, 79518-800-03, 79518-800-04 - Packager: Core Pacific, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 December 3, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DRUG FACTS
- ACTIVE INGREDIENT
- PURPOSE
- Uses:
- WARNINGS:
- DIRECTIONS:
- Other Ingredients:
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SPL UNCLASSIFIED SECTION
• NON-ALCOHOL, WATER-BASED
• ANTI-MICROBIAL PROTECTION
• APPLICABLE ON ALL SURFACES
• DOESN'T DRY OR CRACK SKIN
EFFECTIVELY REDUCE 99.9% COMMON BACTERIA, GERMS & VIRUSES INCLUDING CORONAVIRUS**
12 HOUR SKIN PROTECTION
30 DAY SURFACE PROTECTION
**use as directed at www.doctordumore.com
Manufactured by:
Core Pacific, Inc.
4000 Leeland, St
Houston, TX 77023
www.corepacificinc.com
1-800-860-1637
MADE IN USA.
- Packaging
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INGREDIENTS AND APPEARANCE
DR. DU-MORES VIRAL DEFENSE NANO SILVER SKIN AND SURFACE DISINFECTANT PROTECTANT
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79518-800 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SILVER (UNII: 3M4G523W1G) SODIUM SESQUICARBONATE (UNII: Y1X815621J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79518-800-01 59.14 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/01/2020 2 NDC:79518-800-02 237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/01/2020 3 NDC:79518-800-03 946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/01/2020 4 NDC:79518-800-04 3785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 12/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/01/2020 Labeler - Core Pacific, Inc. (022106593) Establishment Name Address ID/FEI Business Operations Core Pacific, Inc. 022106593 manufacture(79518-800)
