Other
Drug Facts
Distributed by: Previcare Pharmaceutical, Inc.
50 Fountain Plaza • Suite 1400 • Buffalo • NY • 14202 • USA
The following Structured Product Label (SPL) was submitted to the FDA by Previcare Pharmaceutical, Inc. for the product Previcare (NDC 73401-849). 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 other, active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Distributed by: Previcare Pharmaceutical, Inc.
50 Fountain Plaza • Suite 1400 • Buffalo • NY • 14202 • USA
Ethyl Alcohol 70% V/V
Antiseptic
Hand sanitizer to help reduce bacteria that potentially cause disease. For use when soap and water are not available.
For external use only. Flammable. Keep away from heat or flame. Do not ingest. Do not use if you are allergic to any ingredient.
Keep out of reach of children. If swallowed, get medical help. Do not use on open wounds. When using ths product avoid contact with eyes. In case of contact with eyes, rinse thoroughly with water. Stop use and ask a doctor if irritation develops.
Apply to one palm, rub hands together until dry. Use as part of your daily cleaning routine. Do not rinse with water. Do not dilute the product. Supervise children when using this product.
Store at 50-86°F (15-30°C).
Aqua (purified water), Hyssop and Rosemary Mint Oil, Glycerin, Aloe Barbadensis (Aloe) Leaf Juice, PEG-75 Lanolin, PEG-7 Glyceryl Cocoate (emollient), Myristyl Alcohol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine.
Call 1 (716) 427-7979
* Please review the disclaimer below.