maxill Kwiky ET Antiseptic Hand Sanitizer Gel

maxill Kwiky ET Antiseptic Hand Sanitizer Gel by

Drug Labeling and Warnings

maxill Kwiky ET Antiseptic Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by maxill inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MAXILL KWIKY ET ANTISEPTIC HAND SANITIZER GEL- alcohol gel 
maxill inc.

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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maxill Kwiky ET Antiseptic Hand Sanitizer Gel

Active Ingredient

Ethyl Alcohol: 70% v/v

Purpose

Antiseptic

Flammable. Keep away form fire or flame.

For external use only.

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 meidal hekp or contact a Poison Control Center rigth away.

Uses

For use when soap and water are not available. Recommended for repeated use.

Directions:

- Place enough product on hands to cover all surfaces. Rub hands together until dry.

- Supervise children under 6 years of age when they use this product.

Other Information

Store between 15-30°C (59-86°F)

Inactive ingredients

Aminomethyl Propanol, Carbomer, Fragrance, Propylene Glycol, Water

Questions?

1-800-268-8633, www.maxill.com

Uses

Hand sanitizer to help reudce bacteria that potentially can cause disease.

Package Quantity, NDC

475 mL, NDC: 69510-003-02

MAXILL KWIKY ET ANTISEPTIC HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69510-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER 940 (UNII: 4Q93RCW27E)
WATER (UNII: 059QF0KO0R)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69510-003-02	475 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/10/2020
2	NDC: 69510-003-01	50 mL in 1 TUBE; Type 0: Not a Combination Product	07/10/2020
3	NDC: 69510-003-05	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/10/2020
4	NDC: 69510-003-06	4000 mL in 1 JUG; Type 0: Not a Combination Product	07/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/10/2020	08/31/2022

Labeler - maxill inc. (079343581)

Registrant - maxill inc. (248491698)

Establishment
Name	Address	ID/FEI	Business Operations
maxill inc.		248491698	manufacture(69510-003)

Revised: 10/2021

Document Id: ceb47d94-d5ca-f960-e053-2995a90a8b2d

34390-5

Set id: aa17e97f-3656-77ba-e053-2995a90adb15

Version: 2

Effective Time: 20211019