MEDITIME SANITIZING WIPES- benzalkonium chloride cloth

Meditime Sanitizing Wipes by

Drug Labeling and Warnings

Meditime Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Icure Pharmaceutical Inc, Wanju Factory, OTKCNT. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride 0.1%

INACTIVE INGREDIENTS

Water, Cetylpyridinium Chloride, Hydroxyacetophenone, Citric Acid, Aloe Barbadensis Leaf Extract, Butylene Glycol, 1,2-Hexanediol, Tocopheryl Acetate

PURPOSE

ANTISEPTIC

WARNINGS

For external use only. Keep away from heat or flame
--------------------------------------------------------------------------------------------------------
Do not use
in children less than 2 months of age
on open skin wounds
--------------------------------------------------------------------------------------------------------
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Health care personnel wipes to help reduce bacteria.

Directions

■ Wet hands thoroughly with product and allow to dry without wiping
■ Discard wipe in trash receptacle after use
■ Do not flush

Package Label: Meditime Sanitizing Wipes (20sheets)

Package Label: Meditime Sanitizing Wipes (70sheets)

INGREDIENTS AND APPEARANCE

MEDITIME SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73279-0003
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   in 100

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
Hydroxyacetophenone (UNII: G1L3HT4CMH)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
Butylene Glycol (UNII: 3XUS85K0RA)
1,2-Hexanediol (UNII: TR046Y3K1G)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73279-0003-1	20 in 1 PACKET; Type 0: Not a Combination Product	06/01/2020
2	NDC: 73279-0003-2	70 in 1 PACKET; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/01/2020

Labeler - Icure Pharmaceutical Inc, Wanju Factory (695687612)

Registrant - Icure Pharmaceutical Inc, Wanju Factory (695687612)

Establishment
Name	Address	ID/FEI	Business Operations
OTKCNT		694734577	manufacture(73279-0003)