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DRUG FACTS
Lot : 001 | Exp. : 05 / 2020 | NDC: 77110-200-03
Manufactured for and
Distributed by:
Biominerales Pharma, LLC
Boca Raton, Florida 33442
Hand Sanitizer
FDA Label NDC 77110-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Biominerales Pharma, Llc for the product Hand Sanitizer (NDC 77110-200). 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, inactive ingredients, use (s), warnings, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl alcohol (80% v/v)
Purpose
Antimicrobial
Inactive Ingredients
Water(18.025%v/v),Hydrogen Peroxide(0.125%v/v), Carbopol 940 (0.400% v/v), Glycerol (1.450% v/v).
Use (S)
Hand sanitizer to help reduce bacteria on the skin when water and soap are not available.
Warnings
Flammable. Keep away from heat or flame.
For External use only. When using this product keep our of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water for several minutes. Stop use and ask a doctor if irritation or rash occurs for more than 72 hours, consult a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact poison control center right away.
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry.
Principal Display Panel - 236 Ml Bottle Label
BIOMINERALES
PHARMA
Kills more than 99.99% of germs
HAND SANITIZER - GEL
8 oz. (236 mL)
Principal Display Panel (236 mL Bottle Label)
* Please review the disclaimer below.
