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

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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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 not finalpart333A04/09/2018
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 8/2023
Document Id: 027df98e-8a9c-0254-e063-6294a90a350f
Set id: 6971b7de-039d-292f-e053-2a91aa0a26b2
Version: 7
Effective Time: 20230809
 
Medline Industries, LP