Spectrum Health - Amway Hand Sanitizer

Spectrum Health - Amway Hand Sanitizer by

Drug Labeling and Warnings

Spectrum Health - Amway Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Access Business Group LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPECTRUM HEALTH - AMWAY HAND SANITIZER- alcohol gel 
Access Business Group LLC

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Spectrum Health - Amway Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl alcohol 73% v/v

Purpose

Antiseptic

Uses

  • Hand sanitizer to help reduce bacteria that potentially may cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable, keep away from heat or flame.

Do not use

  • In children less than 2 years of age.
  • On open skin woundsOn open skin wounds

When using this product

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

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition.

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 thoroughly into hands for at least 30 seconds. Allow to dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

  • Store between 15-30°C (59-86°F) 
  • Avoid freezing and excessive heat above 40°C (104°F).

Inactive ingredients

Water, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Propylene Glycol, Triethanolamine, Panthenol, Aloe Barbadensis Leaf Juice, Maltodextrin, Sodium Benzoate, Potassium Sorbate

Questions?

USA 1.800.253.6500

Package Labeling:

Label

SPECTRUM HEALTH - AMWAY HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 10056-048
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL73 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TROLAMINE (UNII: 9O3K93S3TK)  
PANTHENOL (UNII: WV9CM0O67Z)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 10056-048-00400 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/202112/31/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)06/01/202112/31/2023
Labeler - Access Business Group LLC (839830713)

Revised: 9/2024
Document Id: 21c44a94-9928-9d5a-e063-6394a90a7af0
Set id: ddd39260-f69e-4c29-9f46-125fc4bf4a84
Version: 3
Effective Time: 20240910