SCRUBS ® Hand Sanitizer Towelette

SCRUBS Hand Sanitizer Towelette by

Drug Labeling and Warnings

SCRUBS Hand Sanitizer Towelette 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 TOWELETTE- benzalkonium chloride cloth 
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 Towelette

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

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

Warnings

For external use only

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if 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

  • Apply to hands
  • Allow skin to dry without wiping

Inactive Ingredients

Water, Ethyl Alcohol, Cocamidopropyl PG-Dimonium Chloride Phosphate, Linear alcohol ethoxylate, Fragrance

PRINCIPAL DISPLAY PANEL - 1.75 mL Towelette Pouch

SCRUBS ®

HAND
SANITIZER
TOWELETTE

  • Kills 99.9% of Germs
  • Conditions & Moisturizes Skin
  • Antibacterial

CONTAINS:
1 PRE-MOISTENED TOWELETTE
8" x 5.5" (20.3 cm x 13.9 cm)

1.75 mL

PRINCIPAL DISPLAY PANEL - 1.75 mL Towelette Pouch
SCRUBS HAND SANITIZER TOWELETTE 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 51239-0949
Route of AdministrationCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
C9-11 PARETH-6 (UNII: KCE0V8JT7W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 51239-0949-11 in 1 POUCH; 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: eff77a14-65b9-2c65-e053-2995a90acf4d
Set id: 7e000cb0-21de-4035-90a4-25b0331b2891
Version: 3
Effective Time: 20221216
 
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