Active Ingredient
Allantoin 0.5%
The following Structured Product Label (SPL) was submitted to the FDA by Genuine Virgin Aloe Corporation for the product Nasal Dryness Relief Gel (NDC 10738-051). 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, don 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.
Allantoin 0.5%
Skin Protectant
For external use only.
do not get into eyes
condition worsens or does not improve within 7 days.
If swallowed get medical help and contact a Poison Control Center right away,.
Apply a thin layer to external nasal passages area(s) as often as needed. May also be used on other facial areas to help relieve disconfort.
For CPAP mask users: Before each use, apply a thin layer to nasal area and wherever mask touches the skin. After each use, apply gel to mask lines to replenish moisture and revitalize skin.
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water, aloe barbadensis (aloe vera) leaf juice*, carbomer, arginine, ethylhexylglycerin, phenoxyethanol.
*Certified Organic Ingredient - Mayacert Certifier
Temporarily protects and helps relieve chapped or cracked skin * Helps protect from the drying effects of wind and cold weather
Nasal Dryness Relief_1oz_label
* Please review the disclaimer below.