MENTHOLATUM MOISTURIZING HAND SANITIZER- benzalkonium chloride gel 
The Mentholatum Company

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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Drug Facts

Active ingredients

Benzalkonium Chloride 0.13%

Purpose

Skin antiseptic

Uses

Warnings

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.

Directions

Inactive ingredients

purified water, hydroxypropyl starch phosphate, lauryl glucoside, dimethicone, chlorphenesin, edetate disodium, glycerin, hyaluronic acid, methyl gluceth-20, phenoxyethanol, polyquaternium-7, rosmarinus officinalis (rosemary) leaf oil, silanetriol

Questions?

1-877-636-2677 MON-FRI 9 AM to 5 PM (EST)

Package/Label Principal Display Panel

Mentholatum Moisturizing Hand Sanitizer

Principal Display Panel

Drug Facts
MENTHOLATUM MOISTURIZING HAND SANITIZER 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-0004
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
WATER (UNII: 059QF0KO0R)  
HYDROXYPROPYL DISTARCH PHOSPHATE, HIGH AMYLOSE CORN (UNII: 9F8ET54T05)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYALURONIC ACID (UNII: S270N0TRQY)  
METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
ROSEMARY OIL (UNII: 8LGU7VM393)  
SILANETRIOL (UNII: E52D0J3TS5)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10742-0004-1192 mL in 1 BOTTLE; Type 0: Not a Combination Product06/12/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/12/2020
Labeler - The Mentholatum Company (002105757)

Revised: 1/2023
Document Id: f28ee215-1dcc-0062-e053-2995a90a6c14
Set id: 365c93bc-2299-4e69-ba3a-69414bfe78d7
Version: 3
Effective Time: 20230118
 
The Mentholatum Company