Oppeal. Hosmall Antibacterial Wipes

Oppeal. Hosmall Antibacterial Wipes by

Drug Labeling and Warnings

Oppeal. Hosmall Antibacterial Wipes by is a Otc medication manufactured, distributed, or labeled by Jiangsu Oppeal Daily Cosmetics Corp. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

OPPEAL. HOSMALL ANTIBACTERIAL WIPES- benzalkonium chloride cloth 
Jiangsu Oppeal Daily Cosmetics Corp. Ltd.

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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Oppeal. Hosmall Antibacterial Wipes

DRUG FACTS

Active Ingredient

Benzalkonium Chloride 0.13%(W/V)

Purpose

Antiseptic

USES

For hand sanitizing to help decrease bacteria on the skin

CAUTIONS

1. For external use only. Avoid contact with eyes or mouth. If contact occurs, rinse eyes thoroughly with warm water. 

Do not use 

on broken skin.

Stop use and ask a doctor 

if irritation or redness occurs.

• Store in a cool, dry place. Avoid heat or direct sunlight.

Keep out of reach of children

Do not flush. Dispose in a trash receptacle.

* Effective at killing 99.9% of germs as Canidia Albicans, Staphylococcus aureus and E.coli in the report Issued by the 3rd party

DIRECTIONS

Tear off the sachet and use as required.

OTHER INFORMATION

Store in a cool, dry place. Avoid heat or direct sunlight.

INACTIVE INGREDIENTS

Aqua(Water), Glycerin, Propylene Glycol, Tocopherol Acetate, Aloe barbadensis Leaf Extract, 1,3-Butylene Glycol, PEG-7 Glyceryl Cocoate, Potassium Sorbate.

Package Labeling:1ct

Package Labeling:5ct

Package Labeling:10ct

OPPEAL. HOSMALL ANTIBACTERIAL WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77828-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77828-005-01	1 in 1 BAG	07/30/2020	12/31/2021
1		3.7 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 77828-005-05	5 in 1 BAG	07/30/2020	12/31/2021
2		4.6 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 77828-005-10	10 in 1 BAG	07/30/2020	12/31/2021
3		4.5 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/30/2020	12/31/2021

Labeler - Jiangsu Oppeal Daily Cosmetics Corp. Ltd. (544096556)

Revised: 1/2022

Document Id: d4ae78cc-e364-1a97-e053-2a95a90a5922

34390-5

Set id: acc65b1e-eeaa-87c5-e053-2995a90af205

Version: 2

Effective Time: 20220103

 

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