ANMEIKANG ALCOHOL WIPES- alcohol wipes cloth

AnMeiKang Alcohol Wipes by

Drug Labeling and Warnings

AnMeiKang Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by Liaoning MeiXin Pharmaceutical Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Alcohol 25% w/w, Benzalkonium chloride 0.05% w/w

Purpose

Antiseptic

Uses

Suitable for wiping hands, face, skin and other unbroken skin.

Warnings

For external use only. Flammable. Keep away from heat or flame.

When using this product avoid to contact eyes, mouth, wounds and other sensitive parts. 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.

The product is insoluble in water, do not dispose the used wet wipes into flush toilets.

Use with caution if you are allergic to alcohol.

The product is disposable, for single use, please do not reuse.

WHEN USING

When using this product avoid to contact eyes, mouth, wounds and other sensitive parts. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Directions

Open the buckle cover, take out the wet wipes, wipe directly on the skin, and close the seal immediately after use to avoid drying of wet wipes.

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.

Other Information

· Store in a cool, dry place, and avoid contact with direct sunlight and heat source.

· Pay attention to environmental protection, please put them into the trash can

Inactive Ingredients

Water, Propylene Glycol, 2-phenoxyethanol

PRINCIPAL DISPLAY PANEL

10PCS, NDC: 81496-001-01

PRINCIPAL DISPLAY PANEL

20PCS, NDC: 81496-001-02

PRINCIPAL DISPLAY PANEL

22PCS, NDC: 81496-001-03

PRINCIPAL DISPLAY PANEL

30PCS, NDC: 81496-001-04

PRINCIPAL DISPLAY PANEL

40PCS, NDC: 81496-001-05

PRINCIPAL DISPLAY PANEL

50PCS, NDC: 81486-001-06

PRINCIPAL DISPLAY PANEL

60PCS, NDC: 81496-001-07

PRINCIPAL DISPLAY PANEL

70PCS, NDC: 81496-001-08

PRINCIPAL DISPLAY PANEL

80PCS, NDC: 81496-001-09

PRINCIPAL DISPLAY PANEL

100PCS, NDC: 81496-001-10

PRINCIPAL DISPLAY PANEL

120PCS, NDC: 81496-001-11

INGREDIENTS AND APPEARANCE

ANMEIKANG ALCOHOL WIPES 
alcohol wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81496-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.8372 g
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.005875 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81496-001-01	10 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
2	NDC: 81496-001-02	20 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
3	NDC: 81496-001-03	22 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
4	NDC: 81496-001-04	30 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
5	NDC: 81496-001-05	40 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
6	NDC: 81496-001-06	50 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
7	NDC: 81496-001-07	60 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
8	NDC: 81496-001-08	70 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
9	NDC: 81496-001-09	80 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
10	NDC: 81496-001-10	100 in 1 BAG; Type 0: Not a Combination Product	02/28/2021
11	NDC: 81496-001-11	120 in 1 BAG; Type 0: Not a Combination Product	02/28/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/28/2021

Labeler - Liaoning MeiXin Pharmaceutical Company (712964681)

Registrant - Liaoning MeiXin Pharmaceutical Company (712964681)

Establishment
Name	Address	ID/FEI	Business Operations
Liaoning MeiXin Pharmaceutical Company		712964681	manufacture(81496-001)