Active Ingredient
Ethyl Alcohol 70% v/v
Panrosa Instant Hand Sanitizer Aloe Vera
FDA Label NDC 50302-013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Panrosa Enterprises, Inc. for the product Panrosa Instant Hand Sanitizer Aloe Vera (NDC 50302-013). 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, do not use, when using this product,, stop use and ask a doctor if, 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
Purpose
Antiseptic
Uses
- hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
- recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from fire or flame.
Do not apply around eyes.
Do Not Use
in ears & mouth.
When Using This Product,
avoid contact with eyes. In case of contact flush eyes with water.
Stop Use And Ask A Doctor If
redness or irritation develop and persist for more than 72 hours.
Keep Out Of Reach Of Children.
Children must be supervised in use of this product.
Directions
- place enough product into your palms and thoroughly spread on both hands.
- rub into skin until dry.
Other Information
- store below 110 ℉ (43℃ ).
- may discolor certain fabrics or surfaces.
Inactive Ingredients
water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, aloe barbadensis leaf juice, tocopheryl acetate, FD&C blue No. 1, FD&C yellow No. 5.
Package Labeling:50302-013-10
Bottle5 (Bottle5)
Package Labeling:50302-013-60
Bottle6 (Bottle6)
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