CVS Health Hand Sanitizer Lotion

CVS Health Hand Sanitizer by

Drug Labeling and Warnings

CVS Health Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Mingshi Technology Co., LTD, Sales and Product Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CVS HEALTH HAND SANITIZER- benzalkonium chloride 0.13% lotion 
Mingshi Technology Co., LTD

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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CVS Health Hand Sanitizer Lotion

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

to help reduce bacteria that potentially can cause disease.
For use when soap is not available

Do Not Use


On children less than 2 months of age on 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 except under adult supervision.

If swallowed, get medical help or contact a poison control Center right away.

Directions

Apply product thoroughly to hands. Rub hands together until absorbed. Do not wipe off or rinse. Apply to hands as needed. Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

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

Inactive ingredients

Water, Glycerin, Tapioca Starch, Polyquaternium-37, Petrolatum, Dicaprylyl Carbonate, Phenoxyethanol, Caprylyl Glycol, Lauryl Glucoside, Trideceth-6, Tocopheryl Acetate, Polymethylsilsesquioxane, Silica, Titanium Dioxide (CI 77891)

CVS Health Hand Sanitizer Lotion

label

CVS HEALTH HAND SANITIZER 
benzalkonium chloride 0.13% lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73992-202
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
STARCH, TAPIOCA (UNII: 24SC3U704I)  
POLYQUATERNIUM-37 (10000 MPA.S) (UNII: 41QWS48DFN)  
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TRIDECYL ETHYLENEGLYCOL MONOETHER (UNII: 36KKG1IWMU)  
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73992-202-05150 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/202112/31/2022
Labeler - Mingshi Technology Co., LTD (542992088)
Registrant - Sales and Product Solutions (037519852)
Establishment
NameAddressID/FEIBusiness Operations
Mingshi Technology Co., LTD542992088manufacture(73992-202)

Revised: 12/2022