Active Ingredient
Ethyl Alcohol 66.5%
Hand Sanitizer
FDA Label NDC 44662-1112
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hopkins Medical for the product Hand Sanitizer (NDC 44662-1112). 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, other, otc - do not use, otc - stop use, 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
Uses
- for handwashing to decrease bacteria on skin
- recommended for repeated use
Other
For external use only
Flammable, keep away from fire or flame
Otc - Do Not Use
Do not use in the eyes. If this happens, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours
Keep Out Of Reach Of Children
If ingested get medical help or contact a Poison Control Center right away
Directions
- wet hands thoroughly with product
- allow to dry without wiping
- children under 6 should be supervised while using this product
Inactive Ingredients
aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine
Principal Display Panel – 1.5 Fl. Oz. Bottle Label
Hopkins
Waterless
Hand
Sanitizer
Enriched with Aloe
Hopkins
Medical Products
Since 1945
1.5 FL OZ (46 ML)
#697373
Principal Display Panel – 1.5 Fl. Oz. Bottle Label (Hop02 0000 01)
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