Otc - Active Ingredient
Active Ingredients
Alcohol 62%
Hand Sanitizer Gel
FDA Label NDC 65692-1003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Raining Rose, Inc. for the product Hand Sanitizer (NDC 65692-1003). 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 otc - active ingredient, otc - purpose, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Warnings
Warnings
Flammable, keep away from open flame and sources of heat. For external use only. Do not ingest.
Do not use in eyes. In case of eye contact flush thoroughly with water and seek medical attention.
Otc - Stop Use
Stop use and ask doctor if irritation and redness develops and persists for more than 72 hours. Do not use if you are allergic to any ingredients.
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.
Dosage & Administration
Directions
- Use 1.5mL and rub thoroughly into hands for at least 30 seconds. Allow to dry.
- Does not require rinsing.
Inactive Ingredient
Inactive Ingredients: Aloe Barbadenis Leaf Juice, Glycerin, Propylene Glycol, Vanilla Fragrance, Water.
Indications & Usage
Use
- Kills some harmful bacteria/germs.
- For occasional use, as needed.
Other Information
- Do not store above 105 F
- May discolor some fabrics.
Package Label.Principal Display Panel
Image Of Bottle Label (Rri)
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