Active Ingredient
Drug Facts
Active Ingredient
Ethyl Alcohol 70% w/w
Saniguard-sf
FDA Label NDC 58575-150
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Inopak. Ltd for the product Saniguard-sf (NDC 58575-150). 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, keep out of reach of children, uses, warnings flammable, keep away from fire or flame., directions, inactive ingredients, saniguard sf label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Keep Out Of Reach Of Children
Keep out of reach of children.
Uses
- For handwashing to decrease bacteria on the skin after changing diapers, assisting ill persons or before contact with a person under medical care or treatment.
- Recommended for repeated use.
Warnings Flammable, Keep Away From Fire Or Flame.
- For external use only. Keep out of eyes, ears or mouth.
- Discontinue use if irritation occurs.
Directions
- If hands are visibly soiled, wash with soap and water and dry hands.
- Wet hands thoroughly with product, especially the area under the fingernails and allow to dry without rinsing.
Inactive Ingredients
benzalkonium chloride, chlorhexidine gluconate, isopropyl alcohol, PEG 10 dimethicone, PEG-14M, phenoxyethanol, polyquaternium 10, water
Saniguard Sf Label
SaniGuard SF
waterless foam hand sanitizer
Compliant with CDC Hand Hygiene Guidlines
Kills more than 99.99% of germs in 15 seconds
Active: Ethyl Alcohol 70%
Does not contain DEA/MEA, triclosan, parabens, formaldehyde, dyes, fragrance
INOPAK LTD. 1-800-762-7725 50ml
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