Hand Sanitizer
FDA Label NDC 77725-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by L.e.d. Cosmetics, Inc. for the product Hand Sanitizer (NDC 77725-002). 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 drug facts:, otc - active ingredient, otc - purpose, directions:, storage and handling, caution:, otc - keep out of reach of children, ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Medicinal Ingredient: Ethyl Alcohol 70%
Otc - Purpose
Purpose: Antiseptic
Directions:
Put a thumbnail size amount in your palm and rub hands briskly until dry.
Note:
Children under 6 years of age should be supervised during use.
Storage And Handling
Do not store above 105°C. May discolor certain fabrics.
Caution:
Flammable. Keep away from fire or flame. For external use only. Keep out of eyes. In case of eye contact, immediately flush with water. If swallowed, call a physician. Discontinue use if irritation or redness develop. If condition persists for more than 72 hours, consult a physician.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Ingredients:
Alcohol (70%), Water(Aqua), Carbomer, Glycerin, Propylene Glycol, Aminomethyl Propanol, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Parfum.
MAY CONTAIN.
Yellow 5 Lake(CI 19140), Red 34 (CI 15880), Red 6 Lake(CI 15850), Ferric Ferrocyanide (CI 77510).
Packaging
Image Description (Label2)
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