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PURELL Advanced Hand Sanitizer be Vibrant

Dosage form: gel
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-028

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.

PURELL Advanced Hand Sanitizer be Vibrant

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame. For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions
  • Place enough product in your palm to thoroughly cover your hands
  • Rub hands together briskly until dry
  • Children under 6 years of age shodl be supervised when using this product

Other information

• Store below 110°F (43°C)

• May discolor certain fabrics or surfaces

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Caprylyl glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Blue 1 (CI 42090), Yellow 5 (CI 19140)

PURELL ADVANCED HAND SANITIZER BE VIBRANT 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-028
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ISOPROPYL ALCOHOL 
CAPRYLYL GLYCOL 
GLYCERIN 
ISOPROPYL MYRISTATE 
.ALPHA.-TOCOPHEROL ACETATE 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
AMINOMETHYLPROPANOL 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:21749-028-0130 mL in 1 PACKAGE
2NDC:21749-028-0259 mL in 1 PACKAGE
3NDC:21749-028-04118 mL in 1 PACKAGE
4NDC:21749-028-08236 mL in 1 PACKAGE
5NDC:21749-028-10295 mL in 1 PACKAGE
6NDC:21749-028-12354 mL in 1 PACKAGE
7NDC:21749-028-45450 mL in 1 PACKAGE
8NDC:21749-028-16473 mL in 1 PACKAGE
9NDC:21749-028-20591 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/22/2016
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-028)

Revised: 12/2016
 
GOJO Industries, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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