Mellow Instant Hand Sanitizer 2 Oz
FDA Label NDC 70108-034
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ashtel Studios, Inc for the product Mellow Instant Hand Sanitizer 2 Oz (NDC 70108-034). 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 drug facts, medicinal ingredient, purpose, features, non medicinal, directions, warning, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Medicinal Ingredient
Ethyl Alcohol 75% (V/V)
Purpose
Antiseptic
Features
♦ To decrease bacteria on the skin that could cause disease.
♦ Recommended for repeated use.
♦ Use anywhere without water.
Non Medicinal
Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Parfum, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, FD&C Yellow No. 5(Tartrazine), FD&C Blue No.1.
Directions
Wet hands thoroughly with product and rub until dry without wiping.
Warning
♦ For external use only-hands, avoid eyes, in case of eye contact flush with water
♦ Flammable. Keep away from heat and flame.
♦ Discontinue if skin becomes irritated and ask a doctor.
Keep Out Of Reach Of Children
In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Packaging
Image (Mel)
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