MOISTURIZER HAND SANITIZER- benzalkonium chloride solution 
Rinati Skin, LLC

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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RINATI - MOISTURIZING HAND SANITIZER (76849-101)

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE 0.13%

PURPOSE

ANTIMICROBIAL

USE

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.

DIRECTIONS

SHAKE WELL BEFORE USE.

SPRAY A SMALL AMOUNT OF PRODUCT INTO PALM OF HAND.

RUB THOROUGHLY OVER ALL SURFACES OF BOTH HANDS.

RUB HANDS TOGETHER BRISKLY UNTIL DRY.

INACTIVE INGREDIENTS

WATER, PROPYLENE GLYCOL, LINUM USITATISSIMUM (FLAX) SEED EXTRACT, OCIMUM TENUIFLORUM LEAF EXTRACT, MELIA AZADIRACHTA LEAF EXTRACT, GLUCONOLACTONE, CITRIC ACID, SODIUM BENZOATE, EUCALYPTUS GLOBULUS OIL

01b LBL_Rinati_Moisturizing Hand Sanitizer 2oz

MOISTURIZER HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76849-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
FLAX SEED (UNII: 4110YT348C)  
OCIMUM TENUIFLORUM TOP (UNII: 34T63W8ULS)  
AZADIRACHTA INDICA LEAF (UNII: HKY915780T)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76849-101-1159 mL in 1 BOTTLE; Type 0: Not a Combination Product05/04/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/04/2020
Labeler - Rinati Skin, LLC (109530208)

Revised: 10/2022
Document Id: ec20cbf3-a0b4-2173-e053-2995a90a3ddd
Set id: 1ea5e840-87b7-4d70-a6f8-502586e4a18e
Version: 3
Effective Time: 20221028
 
Rinati Skin, LLC