SPECTRUM 62% HAND SANITIZER- ethyl alcohol gel 
Medline Industries, LP

----------

214 Spectrum 62% Hand Sanitizer

Active ingredient

Ethyl alcohol 62% v/v

Purpose

Antiseptic

Uses

Warnings

For external use only: hands

Flammable. Keep away from heat and flame.

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor if

  • irritation or redness develops
  • condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

aloe barbadensis leaf juice, carbomer, diisopropylamine, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, water

Manufacturing Information

Manufactured for:

Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA with US and foreign components

www.medline.com

1-800-MEDLINE (633-5463)

REF: HH62G1000

V2 RH22VJO

Package Label

Label V2 RH22VJO

SPECTRUM 62% HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-214
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
DIISOPROPYLAMINE (UNII: BR9JLI40NO)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-214-1359.147 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/201812/06/2022
2NDC:53329-214-70443.6 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/201801/31/2022
3NDC:53329-214-841000 mL in 1 BAG; Type 0: Not a Combination Product04/09/2018
4NDC:53329-214-85354 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)04/09/2018
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 5/2024
Document Id: 199e0f35-6d9a-e028-e063-6294a90ac994
Set id: 6971b7de-039d-292f-e053-2a91aa0a26b2
Version: 8
Effective Time: 20240529
 
Medline Industries, LP