Active Ingredient
Alcohol 75% v/v. Purpose: Antiseptic
75% Alcohol Hand Sanitizer
FDA Label NDC 75617-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jaspers Global Manufacturing Inc for the product 75% Alcohol Hand Sanitizer (NDC 75617-002). 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, uses, warnings, when using this product, stop use and ask a doctor if, 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
Purpose
Antiseptic. Hand senitizer
Uses
- to decrease bacteria on the skin that could cause disease
- recommended for repeated use
Warnings
For external use only: hands
Flammable. Keep away from fire or flame.
When Using This Product
- Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
- Avoid contact with broken skin.
- Do not inhale or ingest
Stop Use And Ask A Doctor If
- irritation or redness develops
- condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep it out of reach of children. If swallowed, get medical help or contact a poison control center right away.
Directions
- wet hands thoroughly with product and allow to dry without wiping.
- for children under 6, use only under adult supervision
- not recommended for infants
Other Information
- do not store above 105F
- may discolor some fabrics
- harmful to wood finishes and plastics
Inactive Ingredients
Acrylic acid polymer, triethanolamine, water
Package Label - Principal Display Panel
500mL NDC: 75617-002-01
Pdp (75617 002 01)
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