Doctors Kline And Green Board Certified Dermatologist Hand Sanitizer Gel
FDA Label NDC 23667-103
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Formulated Solutions, Llc for the product Doctors Kline And Green Board Certified Dermatologist Hand Sanitizer (NDC 23667-103). 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, when using this product, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl alcohol 77% v/v
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
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 110°F (43°C)
- may discolor some fabrics or surfaces
- harmful to wood finished and plastics.
Inactive Ingredients
Ammonium Acryloyldimethyltaurate/VP Copolymer, Caprylic/ Capric Triglyceride, HYdroxyethyl Urea, Tocopheryl Acetate, Water
Package Labeling:
Bottle (Bottle)
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