Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 69366-314
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Honest Company for the product Hand Sanitizer (NDC 69366-314). 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, warnings, otc - keep out of reach of children, directions, inactive ingredients, 8 oz label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antisesptic
Uses
Helps reduce bacteria on the skin
Recommended for repeated use
Warnings
For external use only
Flammable, keep away from fire, sparks, and sources of ignition. Do not store above 104 oF/40 oC
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin
Stop use and ask a doctor if irritation and redness devleop and persist 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 immediately.
Directions
Dispense directly on hands and rub in thoroughly
For children under 6, use adult supervision
Not recommended for infants
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Citric Acid, Glycerin, Hydroxypropyl Guar, Water
8 Oz Label
8 Oz (Handsanitizergel Freeandclear 8oz P101 Page 001)
* Please review the disclaimer below.
