Active Ingredient
Alcohol denat. (anhydrous) 62%
Antiseptic Hand Rub Gel
FDA Label NDC 39892-0412
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by O&m Halyard, Inc. for the product Antiseptic Hand Rub (NDC 39892-0412). 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, use, warnings, stop use and ask a doctor, 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.
Label Section Quick Index
Purpose
Antiseptic
Use
Instant hand antiseptic
Warnings
For external use only. Keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.
Flammable. Keep away from fire or flame.
Stop Use And Ask A Doctor
if significant irritation or sensitization occurs.
Keep Out Of Reach Of Children.
In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.
Directions
- Apply to clean, dry hands
- Wet hands thoroughly with product and allow to dry
Other Information
- Recommended for repeated use
- Reduces bacteria that can potentially cause disease
Inactive Ingredients
Purified water, Carbomer 2020, PPG-20 methyl glucose ether, Carbomer 980, Diisopropanolamine, Fragrance (Lemon), FD&C blue No.1, FD&C yellow No.5
Package Labeling:
Label3 (Label3)
* Please review the disclaimer below.
