ZOVIRO- benzalkonium chloride swab

Zoviro by

Drug Labeling and Warnings

Zoviro by is a Otc medication manufactured, distributed, or labeled by Zoviro, LLC, Jiangsu Xiaolikang Medical Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Benzalkonium chloride 0.13%

PURPOSE

Purpose

Antiseptic

WHEN USING

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

STOP USE

Stop use and ask a doctor if imtaton or redness develops, or if condition persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Inactive ingredients

Water, Glycerin, Ethylhexylglycerin, Phenoxyethanol, Propylene Glycol, Fragrance, Aloe Barbadensis Leaf Extract,Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Aurantium Dulcis (Orange) Oil

DOSAGE & ADMINISTRATION

Directions

Rub hands thoroughly with product and allow to dry.

Children under 2 years old should ask a doctor before use.

INDICATIONS & USAGE

Use

Hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

WARNINGS

Warnings

For external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZOVIRO 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83814-004
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 g

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
BERGAMOT OIL (UNII: 39W1PKE3JI)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ORANGE OIL (UNII: AKN3KSD11B)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83814-004-01	80 in 1 BAG	01/04/2024
1		3.136 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/04/2024

Labeler - Zoviro, LLC (131436286)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangsu Xiaolikang Medical Technology Co., Ltd.		554546867	manufacture(83814-004)