SPECTRUM 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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003 Spectrum Clinical 85%

Active ingredient

Ethyl alcohol 85% v/v

Purpose

Antiseptic

Uses

Warnings

For external use only.

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

acrylates/C10-30 alkyl acrylate crosspolymer, bisabolol, cyclomethicone, glycerin, isohexadecane, myristyl alcohol, povidone, tetrahydroxypropyl ethylenediamine, 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: HH851200G

V2 RB23VJO

Package Label

Front Label V2 RB23VJO

Back Label V2 RB23VJO

SPECTRUM HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL85 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
LEVOMENOL (UNII: 24WE03BX2T)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
POVIDONE (UNII: FZ989GH94E)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
CYCLOMETHICONE (UNII: NMQ347994Z)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-003-1459 mL in 1 BOTTLE; Type 0: Not a Combination Product07/06/201804/30/2023
2NDC:53329-003-70443 mL in 1 BOTTLE; Type 0: Not a Combination Product07/06/201809/30/2020
3NDC:53329-003-841000 mL in 1 BOTTLE; Type 0: Not a Combination Product07/06/201802/17/2023
4NDC:53329-003-741200 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/06/2018
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 8/2023
Document Id: 027df3f1-638a-8b75-e063-6394a90ae96a
Set id: 70598373-bc89-07b9-e053-2991aa0a9e9a
Version: 8
Effective Time: 20230809
 
Medline Industries, LP