Spector & Co Antiseptic Hand Sanitizer with Kiwi Scent

Spector and Co Antiseptic Hand Sanitizer Gel with Kiwi Scent by

Drug Labeling and Warnings

Spector and Co Antiseptic Hand Sanitizer Gel with Kiwi Scent by is a Otc medication manufactured, distributed, or labeled by Spector & Co. Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPECTOR AND CO ANTISEPTIC HAND SANITIZER GEL WITH KIWI SCENT- alcohol gel 
Spector & Co. 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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Spector & Co Antiseptic Hand Sanitizer with Kiwi Scent

Spector & Co Antiseptic Hand Sanitizer Gel with Kiwi Scent

Drug Facts

Active ingredient

Alcohol 65% v/v

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from source of heat, fire or flame.

For external use only.

When using this product

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develops and lasts.

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.

Directions

Directions

• Place enough product in your palm to thoroughly cover your hands and rub hands together until dry.
• Children under 6 years should be supervised when using this product.

Inactive ingredients

Purified water, aloe barbadensis leaf extract, glycerin, aminomethyl propanol, polysorbate 20, carbomer, fragrance

Package Label - Principal Display Panel

Made in Canada

SPECTOR AND CO ANTISEPTIC HAND SANITIZER GEL WITH KIWI SCENT 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90084-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90084-201-01	2 mL in 1 POUCH; Type 0: Not a Combination Product	12/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/18/2020

Labeler - Spector & Co. Inc (203700088)

Revised: 12/2020

Document Id: b6c4fb1f-6016-b73e-e053-2a95a90ae645

34390-5

Set id: b6c4fd9b-cf89-781f-e053-2a95a90ab9ef

Version: 1

Effective Time: 20201218