PORTABLE DEGERMING WIPE- alcohol cloth

portable degerming wipe by

Drug Labeling and Warnings

portable degerming wipe by is a Otc medication manufactured, distributed, or labeled by Dalian Aikangning Biological Technology Co. LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Main materials

Alcohol, Benzalkonium chloride

SPL UNCLASSIFIED SECTION

Size: 200mm x 150mm Number: 30 pieces

Sanitation standard: GB15979

Executive standard: GB/127728
Saniltation license: Liaoning province health department degerming product certificate No. (2018) B003
Expiration date: 24 months

PURPOSE

degerming

usage method

• Open the front sealing paste, and then draw out the wipes for use.
• Please use it as soon as possible affer opening
• After opening, please stick the seal well to prevent drying

Attention

• In case of any skin discomfort during use, please stop using immediately and go to the doctor in time
• Please don't use it in parts with mucous membrane such as eyes or mouth
• Keep it away from infants.
• Avoid direct sunlight or high temperature
• This produdt is water-insoluble non-wovon fabric, can not be directly thrown into the toilet.

DO NOT USE

Please don't use it in parts with mucous membrane such as eyes or mouth

WHEN USING

degerming

STOP USE

In case of any skin discomfort during use, please stop using immediately and go to the doctor in time

KEEP OUT OF REACH OF CHILDREN

Keep it away from infants.

DOSAGE & ADMINISTRATION

Open the front sealing paste, and then draw out the wipes for use.

STORAGE AND HANDLING

expiration date:24 months

Avoid direct sunlight or high temperature

INACTIVE INGREDIENT

water, Propylene Glycol

PRINCIPAL DISPLAY PANEL

10 pcs: 81613-001-01

20 pcs: 81613-001-02

30 pcs: 81613-001-03

60 pcs: 81613-001-04

80 pcs: 81613-001-05

100 pcs: 81613-001-06

120 pcs: 81613-001-07

INGREDIENTS AND APPEARANCE

PORTABLE DEGERMING WIPE 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81613-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	30 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81613-001-01	18 mL in 1 BAG; Type 0: Not a Combination Product	03/20/2020
2	NDC: 81613-001-02	36 mL in 1 BAG; Type 0: Not a Combination Product	03/20/2020
3	NDC: 81613-001-03	48 mL in 1 BAG; Type 0: Not a Combination Product	03/20/2020
4	NDC: 81613-001-04	108 mL in 1 BAG; Type 0: Not a Combination Product	03/20/2020
5	NDC: 81613-001-05	144 mL in 1 BAG; Type 0: Not a Combination Product	03/20/2020
6	NDC: 81613-001-06	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/20/2020
7	NDC: 81613-001-07	216 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/20/2020

Labeler - Dalian Aikangning Biological Technology Co. LTD (540960683)

Establishment
Name	Address	ID/FEI	Business Operations
Dalian Aikangning Biological Technology Co. LTD		540960683	manufacture(81613-001) , label(81613-001)