Nuit D Orient Hand Sanitizer
FDA Label NDC 79877-065
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Paris Perfumes, Inc. for the product Nuit D Orient Hand Sanitizer (NDC 79877-065). 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 drug facts, active ingredient, purpose, uses, warnings, otc - 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
Active Ingredient
Ethyl alcohol 65%
Purpose
Antiseptic
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 and redness develop ■ condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep 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 105 F ■ may discolor some fabrics ■ harmful to wood finishes and plastics.
Inactive Ingredients
deoinized water, carbomer, triethanolamine, aloe vera gel (aloe barbadensis leaf juice)
Packaging
Image (7987706516)
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