Active Ingredient
BENZALKONIUM CHLORIDE 0.13%
Moisturizer Hand Sanitizer
FDA Label NDC 76849-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rinati Skin, Llc for the product Moisturizer Hand Sanitizer (NDC 76849-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
Otc - Keep Out Of Reach Of Children
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
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