SCRUBS ® Hand Sanitizer Gel

SCRUBS Hand Sanitizer by

Drug Labeling and Warnings

SCRUBS Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by ITW Pro Brands, Celeste Industries Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SCRUBS HAND SANITIZER- alcohol gel 
ITW Pro Brands

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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SCRUBS ® Hand Sanitizer Gel

Drug Facts

Active Ingredient

Ethyl Alcohol 62.5%

Purpose

Antimicrobial

Uses

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

  • For external use only.

  • Keep out of reach of children.
  • Flammable. Keep away from open flame and sources of heat.

  • Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

  • When using this product, avoid contact with eyes. In case of eye contact, flush eyes with water.
  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

Inactive Ingredients

Aqua, PEG-4 Diheptanoate, Acrylates/C10-30 Alkyl Acrylate crosspolymer, Fragrance, Aminomethyl Propanol (May contain hydroxypropylcellulose)

Other Information

  • Store below 110°F (43°C).
  • May discolor certain fabrics or surfaces

PRINCIPAL DISPLAY PANEL - 237 mL Bottle Label

SCRUBS ®
HAND
SANITIZER
GEL

  • Kills 99% of Germs on Contact
  • Requires No Water or Towels
  • Apply Small Amount to Hands and
    Rub until Dry

WITH 62.5%
ALCOHOL

CAUTION: Use on Hands Only
8 fl oz (237 mL)

PRINCIPAL DISPLAY PANEL - 237 mL Bottle Label
SCRUBS HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 51239-0429
Route of AdministrationCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.625 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PEG-4 DIHEPTANOATE (UNII: 2DQ7O61VHJ)  
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 51239-0429-1177 mL in 1 BOTTLE; Type 0: Not a Combination Product11/13/202011/14/2022
2NDC: 51239-0429-2177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/13/202011/14/2022
3NDC: 51239-0429-3237 mL in 1 BOTTLE; Type 0: Not a Combination Product11/13/202011/14/2022
4NDC: 51239-0429-4237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/13/202011/14/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/13/202011/14/2022
Labeler - ITW Pro Brands (067952994)
Registrant - Celeste Industries Corporation (047795034)

Revised: 12/2022
Document Id: eff751f9-5cc8-a55e-e053-2995a90a1daf
Set id: 494af9fa-1f1c-4475-b470-07cad7858243
Version: 3
Effective Time: 20221216
 
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