Purpose
Antimicrobial
Hand Sanitizer Foam
FDA Label NDC 72471-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vmp Cosmetics, Llc for the product Hand Sanitizer Foam (NDC 72471-100). 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 purpose, uses, warnings, stop use, keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
*To help decrease bacterial on the skin. Recomended for repeated use as needed.
Warnings
For external use only.
Stop Use
*Stop use and consult with doctor if irritation and redness develops, or if condition persists for more than 24 hours.
Keep Out Of Reach Of Children
In case of accidental ingestion, seek professional assistance or contact a poison Control Center immediately.
Directions
* Pump a sufficient amount of foam into palm of hand.
* Rub thoroughly over all surfaces of both hands.
* Rub hands repeatedly until dry.
Other Information
Do not store above 104 OF.
Inactive Ingredients
Water, Glycerin, Hyaluronic Acid, Aloe Barbadensis Leaf Juice Powder, Quillaja Saponaria (Soapbark) Bark Extract, PEG-8 Dimethicone, Polyquaternium-7, PPG-26 Buteth-26, PEG-40 Hydrogenated Castor Oil, Sodium Decylglucosides Hydroxypropylsulfonate, Ethylhexylglycerin, Phenoxyethanol, Fragrance.
Active Ingredient
Benzalkonium Chloride 0.13%
Pdp
MEDILAB
365
HAND SANITIZER FOAM
ANTI-BACTERIAL
ADVANCED FORMULA
KILLS 99.99%
OF GERMS
REGISTERED CERTIFIED
FDA GMP
FORMULA FACILITY
1.7 FL.OZ (50 ML)
* Please review the disclaimer below.
