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Daylogic Foaming Sanitizer Aloe

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1mg in 1mL
Labeler: RITE AID CORPORATION
NDC Code: 11822-2440

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.

DRUG FACTS

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Uses

to help decrease bacteria on the skin.

Warnings

For external use only

When using this product

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or redness develops and lasts.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions
  • Pump enough product on your palm to thoroughly cover your hands, rub together until dry.
  • Children under 6 years should be supervised when using this product.

Inactive ingredients

Water (Aqua), Polysorbate 20, Ethylhexyl Methoxycinnamate, Buty Methoxydibenzoylmethane, Ethylhexyl Salicyalte, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Camellia Sinensis Leaf Extract, DMDM Hydantoin, Sodium Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Yellow 5 (CI 19140).

Label Copy

DAYLOGIC FOAMING SANITIZER ALOE 
benzalkonium chlolride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-2440
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
POLYSORBATE 20 
OCTINOXATE 
AVOBENZONE 
OCTISALATE 
PPG-26-BUTETH-26 
POLYOXYL 40 HYDROGENATED CASTOR OIL 
ALOE VERA LEAF 
GREEN TEA LEAF 
DMDM HYDANTOIN 
SODIUM HYDROXIDE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:11822-2440-8237 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/09/2016
Labeler - RITE AID CORPORATION (014578892)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIOperations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(11822-2440)

 
RITE AID CORPORATION

Medically reviewed on Feb 12, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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