Drug Facts

EZPHARM HAND SANITIZING TISSUE- benzalkonium liquid
WOOIL C&TECH.CORP

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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Drug Facts

benzalkonium

Water, Glycerin, Polysorbate 80, Sodium Benzonate, Citric Acid, Maltodextrin, Aloe Barbadensis Leaf Juice Powder, Fragrance, Tocopheryl Acetate

■ To decrease bacteria on the skin that could cause disease

■ Recommended for repeated use

KEEP OUT OF REACH OF THE CHILDREN

■ Wipe hands thoroughly with product and allow to dry.

■ Discard wipe in trash. Do not flush.

■ keep out of eyes. In case of contact with eyes, flush thoroughly with water.

■ avoid contact with broken skin.

■ do not inhale or ingest.

external use only

label

EZPHARM HAND SANITIZING TISSUE
benzalkonium liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:58474-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:58474-001-01	80 mL in 1 PACKAGE; Type 0: Not a Combination Product	07/11/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	07/11/2020

Labeler - WOOIL C&TECH.CORP (688331078)

Registrant - WOOIL C&TECH.CORP (688331078)

Name	Address	ID/FEI	Business Operations
Establishment
WOOIL C&TECH.CORP		688331078	manufacture(58474-001)