VIPY ANTIBACTERIAL SANITIZING WET WIPES SWAB- benzalkonium chloride cloth swab
VIP SALES & MARKETING LLC
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.
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VIPY ANTIBACTERIAL SANITIZING WET WIPES - benzalkonium chloride cloth - swab
ACTIVE INGREDIENT
Benzalkonium Chloride 0.15%
USES
- For hand washing to decrease bacteria on the skin. Recommended for repeat use.
WARNINGS
- For external use only.
- Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.
Do not use
- if you are allergic to any of the ingredients.
- Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.
- Do not use in children under 2 months of age.
DIRECTIONS OF USE
- Open resealable label and pull one sheet from pack. Thoroughly clean hands or affected area and discard in receptacle, and do not flush. Allow to dry without wiping. Be sure to reseal label complete to retain moisture.
OTHER INFORMATION
- Store at room temperature.
KEEP OUT OF REACH OF CHILDREN
- unless under adult supervision.
- If swallowed, get medical help, or contact a Poison Control Center immediately.
INACTIVE INGREDIENTS
- Water (Aqua), Aloe Barbadensis Leaf Juice, Allantoin, Benzoic Acid, Citric Acid, Cocamidopropyl Betaine, Dehydroacedic Acid, Dicaprylyl Carbonate, Glycerin, Glyceryl Oleate, Lauryl Glucoside, Olus Oil, Panthenol, Parfum, Phenoxyethanol, Polyglyceryl-2-Dipolyhydroxystearate, Polysorbate 20, Propylene Glycol, Tocopheryl Acetate
80660-002-80 PACKAGE LABELING: ANTIBACTERIAL SANITIZING 80 WIPES
![Antibacterial Sanitizing 80 Wipes](https://fda.report/DailyMed/b0164a6c-3021-3d6d-e053-2995a90a43d8/80660-002-80+PACKAGE+LABELING.jpg)
VIPY ANTIBACTERIAL SANITIZING WET WIPES
SWAB
benzalkonium chloride cloth swab |
Product Information |
Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC: 80660-002 |
Route of Administration | TOPICAL |
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Active Ingredient/Active Moiety |
Ingredient Name | Basis of Strength | Strength |
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) | BENZALKONIUM CHLORIDE | 0.15 g in 100 g |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 80660-002-80 | 80 in 1 BAG | 09/30/2020 | |
1 | | 5.67 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) | | |
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Marketing Information |
Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
OTC monograph not final | part333E | 09/30/2020 | 12/31/2022 |
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Labeler - VIP SALES & MARKETING LLC
(117675612)
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