HAND SANITIZER- alcohol liquid
Navajo Manufacturing Company 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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Handy Solutions Hand Sanitizer

Active ingredient

Ethyl Alcohol 62%

Uses

A hand sanitizer to help reduce bacteria on the skin

For external use only.

Flammable. Keep away from fire or flame or sparks

When using this product do not use in or near eyes, in case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears on the skin.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

• Open cap, place a small amount (enough to cover both hands) in palm of your hand.

• Rub hands together, spreading the sanitizer and rubbing vigorously until dry.

• Children under 6 years of age should be supervised by an adult when applying this product.

Purified Water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, carbomer, aloe barbadensis leaf juice, fragrance

Purpose

Antiseptic

HAND SANITIZER
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67751-011
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	6.2 mL in 10 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER 1342 (UNII: 809Y72KV36)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:67751-011-03	10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/30/2011	08/04/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	06/30/2011	08/04/2016

Labeler - Navajo Manufacturing Company Inc. (091917799)

Registrant - Ningbo Pulisi Daily Chemical Products Co., Ltd. (529047265)

Name	Address	ID/FEI	Business Operations
Establishment
Ningbo Pulisi Daily Chemical Products Co., Ltd.		529047265	manufacture(67751-011)

Revised: 11/2018

Document Id: 7bc0e390-e352-8685-e053-2a91aa0a8b96

Set id: 90d00622-bac3-4d5f-a3bc-64a0b585d8e1

Version: 2

Effective Time: 20181128

Navajo Manufacturing Company Inc.