RINSE-FREE Hand Sanitizer

FREE Hand Sanitizer by

Drug Labeling and Warnings

FREE Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by BLAKEMORE SALES CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FREE HAND SANITIZER- alcohol gel 
BLAKEMORE SALES CORPORATION

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RINSE-FREE Hand Sanitizer

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

  • helps reduce bacteria that potentially can cause disease
  • helps prevent cross contamination by hand contact
  • recommended for repeated use

Warnings

For external use only.

Flammable. Keep away from heat or flame.

Do not use

  • in children less than 2 months of age or on open skin wounds

When using this product

  • keep out of eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or redness develops.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Place enough product on hands to cover all surfaces.
  • Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

  • avoid freezing and excessive heat above 40°C(104°F)
  • may disolor certain fabrics

Inactive ingredients

Water, Glycerin, Aloe Barbadensis Extract, Aminomethyl Propanol, Propylene Glycol, Carbomer, Fragrance, Tocopherol.

Package Labeling

Label

FREE HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78304-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78304-005-01500 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package05/22/202001/31/2026
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/22/202001/31/2026
Labeler - BLAKEMORE SALES CORPORATION (164380578)

Revised: 1/2024
Document Id: 0fb5044e-3abe-1805-e063-6394a90a810b
Set id: 3a4537bf-fb59-489a-a147-a80732cac2df
Version: 2
Effective Time: 20240124