Handy Solutions Hand Sanitizer

Handy Solutions Hand Sanitizer

Drug Labeling and Warnings

Drug Details

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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%

Purpose

Antiseptic

Uses

A hand sanitizer to help reduce bacteria on the skin.

Warnings

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.

Directions

Place enough to cover both hands in the palm, and rub hands together until dry.

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

Other Information

Store below 110°F (43­°C).

May discolor certain fabrics or surfaces.

Inactve ingredients

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

Questions or comments?

Call 1-800-525-5097

HandSanitizer

HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 67751-011
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL36.58 mL  in 59 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 67751-011-0459 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/01/2011
Labeler - Navajo Manufacturing Company Inc. (091917799)
Registrant - Ningbo Pulisi Daily Chemical Products Co., Ltd. (529047265)
Establishment
NameAddressID/FEIBusiness Operations
Navajo Manufacturing Company Inc.136941411relabel(67751-011) , repack(67751-011)
Establishment
NameAddressID/FEIBusiness Operations
Ningbo Pulisi Daily Chemical Products Co., Ltd.529047265manufacture(67751-011)

Revised: 11/2019
 
Navajo Manufacturing Company Inc.


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